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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs5956

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr7:80663133 (GRCh38.p14) Help

The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.

Alleles
G>A
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.014844 (3929/264690, TOPMED)
A=0.018763 (4714/251244, GnomAD_exome)
A=0.023187 (4068/175446, ALFA) (+ 24 more)
A=0.019469 (2728/140120, GnomAD)
A=0.019080 (2315/121332, ExAC)
A=0.00576 (453/78700, PAGE_STUDY)
A=0.00025 (7/28258, 14KJPN)
A=0.00018 (3/16758, 8.3KJPN)
A=0.01899 (247/13006, GO-ESP)
A=0.0083 (53/6404, 1000G_30x)
A=0.0088 (44/5008, 1000G)
A=0.0426 (191/4480, Estonian)
A=0.0257 (99/3854, ALSPAC)
A=0.0280 (104/3708, TWINSUK)
A=0.0007 (2/2922, KOREAN)
A=0.0088 (10/1136, Daghestan)
A=0.0129 (14/1088, HapMap)
A=0.033 (33/998, GoNL)
A=0.022 (13/600, NorthernSweden)
A=0.013 (7/534, MGP)
A=0.062 (19/304, FINRISK)
A=0.009 (2/216, Qatari)
A=0.03 (1/40, GENOME_DK)
G=0.5 (2/4, SGDP_PRJ)
A=0.5 (2/4, SGDP_PRJ)
G=0.5 (1/2, Siberian)
A=0.5 (1/2, Siberian)
Clinical Significance
Reported in ClinVar
Gene : Consequence
CD36 : Synonymous Variant
Publications
5 citations
Genomic View
See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541
Population Group Sample Size Ref Allele Alt Allele
Total Global 191808 G=0.977113 A=0.022887
European Sub 161484 G=0.975255 A=0.024745
African Sub 12582 G=0.99491 A=0.00509
African Others Sub 434 G=1.000 A=0.000
African American Sub 12148 G=0.99473 A=0.00527
Asian Sub 722 G=1.000 A=0.000
East Asian Sub 560 G=1.000 A=0.000
Other Asian Sub 162 G=1.000 A=0.000
Latin American 1 Sub 1046 G=0.9885 A=0.0115
Latin American 2 Sub 2282 G=0.9930 A=0.0070
South Asian Sub 192 G=1.000 A=0.000
Other Sub 13500 G=0.97763 A=0.02237


Help

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download
Study Population Group Sample Size Ref Allele Alt Allele
TopMed Global Study-wide 264690 G=0.985156 A=0.014844
gnomAD - Exomes Global Study-wide 251244 G=0.981237 A=0.018763
gnomAD - Exomes European Sub 135212 G=0.969307 A=0.030693
gnomAD - Exomes Asian Sub 48980 G=0.99761 A=0.00239
gnomAD - Exomes American Sub 34592 G=0.99500 A=0.00500
gnomAD - Exomes African Sub 16256 G=0.99539 A=0.00461
gnomAD - Exomes Ashkenazi Jewish Sub 10074 G=0.99216 A=0.00784
gnomAD - Exomes Other Sub 6130 G=0.9804 A=0.0196
Allele Frequency Aggregator Total Global 175446 G=0.976813 A=0.023187
Allele Frequency Aggregator European Sub 151394 G=0.975369 A=0.024631
Allele Frequency Aggregator Other Sub 12066 G=0.97771 A=0.02229
Allele Frequency Aggregator African Sub 7744 G=0.9946 A=0.0054
Allele Frequency Aggregator Latin American 2 Sub 2282 G=0.9930 A=0.0070
Allele Frequency Aggregator Latin American 1 Sub 1046 G=0.9885 A=0.0115
Allele Frequency Aggregator Asian Sub 722 G=1.000 A=0.000
Allele Frequency Aggregator South Asian Sub 192 G=1.000 A=0.000
gnomAD - Genomes Global Study-wide 140120 G=0.980531 A=0.019469
gnomAD - Genomes European Sub 75860 G=0.96876 A=0.03124
gnomAD - Genomes African Sub 42014 G=0.99503 A=0.00497
gnomAD - Genomes American Sub 13650 G=0.99311 A=0.00689
gnomAD - Genomes Ashkenazi Jewish Sub 3320 G=0.9922 A=0.0078
gnomAD - Genomes East Asian Sub 3126 G=1.0000 A=0.0000
gnomAD - Genomes Other Sub 2150 G=0.9865 A=0.0135
ExAC Global Study-wide 121332 G=0.980920 A=0.019080
ExAC Europe Sub 73330 G=0.97110 A=0.02890
ExAC Asian Sub 25118 G=0.99745 A=0.00255
ExAC American Sub 11572 G=0.99447 A=0.00553
ExAC African Sub 10404 G=0.99510 A=0.00490
ExAC Other Sub 908 G=0.981 A=0.019
The PAGE Study Global Study-wide 78700 G=0.99424 A=0.00576
The PAGE Study AfricanAmerican Sub 32514 G=0.99373 A=0.00627
The PAGE Study Mexican Sub 10810 G=0.99510 A=0.00490
The PAGE Study Asian Sub 8318 G=0.9996 A=0.0004
The PAGE Study PuertoRican Sub 7918 G=0.9922 A=0.0078
The PAGE Study NativeHawaiian Sub 4534 G=0.9949 A=0.0051
The PAGE Study Cuban Sub 4230 G=0.9922 A=0.0078
The PAGE Study Dominican Sub 3828 G=0.9950 A=0.0050
The PAGE Study CentralAmerican Sub 2450 G=0.9959 A=0.0041
The PAGE Study SouthAmerican Sub 1982 G=0.9939 A=0.0061
The PAGE Study NativeAmerican Sub 1260 G=0.9754 A=0.0246
The PAGE Study SouthAsian Sub 856 G=0.996 A=0.004
14KJPN JAPANESE Study-wide 28258 G=0.99975 A=0.00025
8.3KJPN JAPANESE Study-wide 16758 G=0.99982 A=0.00018
GO Exome Sequencing Project Global Study-wide 13006 G=0.98101 A=0.01899
GO Exome Sequencing Project European American Sub 8600 G=0.9737 A=0.0263
GO Exome Sequencing Project African American Sub 4406 G=0.9952 A=0.0048
1000Genomes_30x Global Study-wide 6404 G=0.9917 A=0.0083
1000Genomes_30x African Sub 1786 G=0.9989 A=0.0011
1000Genomes_30x Europe Sub 1266 G=0.9660 A=0.0340
1000Genomes_30x South Asian Sub 1202 G=0.9975 A=0.0025
1000Genomes_30x East Asian Sub 1170 G=1.0000 A=0.0000
1000Genomes_30x American Sub 980 G=0.995 A=0.005
1000Genomes Global Study-wide 5008 G=0.9912 A=0.0088
1000Genomes African Sub 1322 G=0.9977 A=0.0023
1000Genomes East Asian Sub 1008 G=1.0000 A=0.0000
1000Genomes Europe Sub 1006 G=0.9652 A=0.0348
1000Genomes South Asian Sub 978 G=0.997 A=0.003
1000Genomes American Sub 694 G=0.996 A=0.004
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.9574 A=0.0426
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.9743 A=0.0257
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.9720 A=0.0280
KOREAN population from KRGDB KOREAN Study-wide 2922 G=0.9993 A=0.0007
Genome-wide autozygosity in Daghestan Global Study-wide 1136 G=0.9912 A=0.0088
Genome-wide autozygosity in Daghestan Daghestan Sub 628 G=0.989 A=0.011
Genome-wide autozygosity in Daghestan Near_East Sub 144 G=1.000 A=0.000
Genome-wide autozygosity in Daghestan Central Asia Sub 122 G=0.992 A=0.008
Genome-wide autozygosity in Daghestan Europe Sub 108 G=0.991 A=0.009
Genome-wide autozygosity in Daghestan South Asian Sub 98 G=1.00 A=0.00
Genome-wide autozygosity in Daghestan Caucasus Sub 36 G=0.97 A=0.03
HapMap Global Study-wide 1088 G=0.9871 A=0.0129
HapMap American Sub 424 G=0.976 A=0.024
HapMap African Sub 402 G=0.998 A=0.002
HapMap Europe Sub 174 G=0.983 A=0.017
HapMap Asian Sub 88 G=1.00 A=0.00
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.967 A=0.033
Northern Sweden ACPOP Study-wide 600 G=0.978 A=0.022
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 G=0.987 A=0.013
FINRISK Finnish from FINRISK project Study-wide 304 G=0.938 A=0.062
Qatari Global Study-wide 216 G=0.991 A=0.009
The Danish reference pan genome Danish Study-wide 40 G=0.97 A=0.03
SGDP_PRJ Global Study-wide 4 G=0.5 A=0.5
Siberian Global Study-wide 2 G=0.5 A=0.5
Help

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements
Sequence name Change
GRCh38.p14 chr 7 NC_000007.14:g.80663133G>A
GRCh37.p13 chr 7 NC_000007.13:g.80292449G>A
CD36 RefSeqGene NG_008192.1:g.65946G>A
Gene: CD36, CD36 molecule (plus strand)
Molecule type Change Amino acid[Codon] SO Term
CD36 transcript variant 7 NM_001289909.1:c.430-1273…

NM_001289909.1:c.430-1273G>A

 		N/A Intron Variant
CD36 transcript variant 3 NM_000072.3:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform 1 NP_000063.2:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant 6 NM_001289908.1:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform 2 NP_001276837.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant 2 NM_001001547.3:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform 1 NP_001001547.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant 8 NM_001289911.2:c.345G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform 4 NP_001276840.1:p.Pro115= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant 5 NM_001127444.2:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform 1 NP_001120916.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant 10 NM_001371074.1:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform 1 NP_001358003.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant 14 NM_001371079.1:c.471G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform 5 NP_001358008.1:p.Pro157= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant 13 NM_001371078.1:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform 1 NP_001358007.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant 16 NM_001371081.1:c.108G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform 6 NP_001358010.1:p.Pro36= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant 15 NM_001371080.1:c.108G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform 6 NP_001358009.1:p.Pro36= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant 12 NM_001371077.1:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform 1 NP_001358006.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant 11 NM_001371075.1:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform 1 NP_001358004.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant 4 NM_001127443.2:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform 1 NP_001120915.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant 1 NM_001001548.3:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform 1 NP_001001548.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant 9 NR_110501.1:n.752G>A N/A Non Coding Transcript Variant
CD36 transcript variant X1 XM_005250715.6:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform X1 XP_005250772.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant X2 XM_047421041.1:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform X1 XP_047276997.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant X3 XM_047421042.1:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform X1 XP_047276998.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant X4 XM_047421043.1:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform X1 XP_047276999.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant X5 XM_024447002.2:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform X1 XP_024302770.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant X6 XM_047421044.1:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform X1 XP_047277000.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant X7 XM_024447003.2:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform X1 XP_024302771.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant X8 XM_047421045.1:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform X1 XP_047277001.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant X9 XM_047421046.1:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform X1 XP_047277002.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant X10 XM_047421047.1:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform X1 XP_047277003.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant X11 XM_047421048.1:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform X1 XP_047277004.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
CD36 transcript variant X12 XM_047421049.1:c.573G>A P [CCG] > P [CCA] Coding Sequence Variant
platelet glycoprotein 4 isoform X1 XP_047277005.1:p.Pro191= P (Pro) > P (Pro) Synonymous Variant
Help

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Allele: A (allele ID: 898429 )
ClinVar Accession Disease Names Clinical Significance
RCV001162667.2 Platelet-type bleeding disorder 10 Uncertain-Significance
RCV001675985.2 not provided Benign
Help

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement G= A
GRCh38.p14 chr 7 NC_000007.14:g.80663133= NC_000007.14:g.80663133G>A
GRCh37.p13 chr 7 NC_000007.13:g.80292449= NC_000007.13:g.80292449G>A
CD36 RefSeqGene NG_008192.1:g.65946= NG_008192.1:g.65946G>A
CD36 transcript variant 1 NM_001001548.3:c.573= NM_001001548.3:c.573G>A
CD36 transcript variant 1 NM_001001548.2:c.573= NM_001001548.2:c.573G>A
CD36 transcript variant 3 NM_000072.3:c.573= NM_000072.3:c.573G>A
CD36 transcript variant 2 NM_001001547.3:c.573= NM_001001547.3:c.573G>A
CD36 transcript variant 2 NM_001001547.2:c.573= NM_001001547.2:c.573G>A
CD36 transcript variant 5 NM_001127444.2:c.573= NM_001127444.2:c.573G>A
CD36 transcript variant 5 NM_001127444.1:c.573= NM_001127444.1:c.573G>A
CD36 transcript variant 4 NM_001127443.2:c.573= NM_001127443.2:c.573G>A
CD36 transcript variant 4 NM_001127443.1:c.573= NM_001127443.1:c.573G>A
CD36 transcript variant 8 NM_001289911.2:c.345= NM_001289911.2:c.345G>A
CD36 transcript variant 8 NM_001289911.1:c.345= NM_001289911.1:c.345G>A
CD36 transcript variant 11 NM_001371075.1:c.573= NM_001371075.1:c.573G>A
CD36 transcript variant 12 NM_001371077.1:c.573= NM_001371077.1:c.573G>A
CD36 transcript variant 16 NM_001371081.1:c.108= NM_001371081.1:c.108G>A
CD36 transcript variant 10 NM_001371074.1:c.573= NM_001371074.1:c.573G>A
CD36 transcript variant 13 NM_001371078.1:c.573= NM_001371078.1:c.573G>A
CD36 transcript variant 14 NM_001371079.1:c.471= NM_001371079.1:c.471G>A
CD36 transcript variant 9 NR_110501.1:n.752= NR_110501.1:n.752G>A
CD36 transcript variant 6 NM_001289908.1:c.573= NM_001289908.1:c.573G>A
CD36 transcript variant 15 NM_001371080.1:c.108= NM_001371080.1:c.108G>A
CD36 transcript variant X1 XM_005250715.6:c.573= XM_005250715.6:c.573G>A
CD36 transcript variant X1 XM_005250715.5:c.573= XM_005250715.5:c.573G>A
CD36 transcript variant X1 XM_005250715.4:c.573= XM_005250715.4:c.573G>A
CD36 transcript variant X1 XM_005250715.3:c.573= XM_005250715.3:c.573G>A
CD36 transcript variant X3 XM_005250715.2:c.573= XM_005250715.2:c.573G>A
CD36 transcript variant X3 XM_005250715.1:c.573= XM_005250715.1:c.573G>A
CD36 transcript variant X7 XM_024447003.2:c.573= XM_024447003.2:c.573G>A
CD36 transcript variant X5 XM_024447003.1:c.573= XM_024447003.1:c.573G>A
CD36 transcript variant X5 XM_024447002.2:c.573= XM_024447002.2:c.573G>A
CD36 transcript variant X2 XM_024447002.1:c.573= XM_024447002.1:c.573G>A
CD36 transcript variant X11 XM_047421048.1:c.573= XM_047421048.1:c.573G>A
CD36 transcript variant X9 XM_047421046.1:c.573= XM_047421046.1:c.573G>A
CD36 transcript variant X2 XM_047421041.1:c.573= XM_047421041.1:c.573G>A
CD36 transcript variant X6 XM_047421044.1:c.573= XM_047421044.1:c.573G>A
CD36 transcript variant X8 XM_047421045.1:c.573= XM_047421045.1:c.573G>A
CD36 transcript variant X3 XM_047421042.1:c.573= XM_047421042.1:c.573G>A
CD36 transcript variant X4 XM_047421043.1:c.573= XM_047421043.1:c.573G>A
CD36 transcript variant X12 XM_047421049.1:c.573= XM_047421049.1:c.573G>A
CD36 transcript variant X10 XM_047421047.1:c.573= XM_047421047.1:c.573G>A
platelet glycoprotein 4 isoform 1 NP_001001548.1:p.Pro191= NP_001001548.1:p.Pro191=
platelet glycoprotein 4 isoform 1 NP_000063.2:p.Pro191= NP_000063.2:p.Pro191=
platelet glycoprotein 4 isoform 1 NP_001001547.1:p.Pro191= NP_001001547.1:p.Pro191=
platelet glycoprotein 4 isoform 1 NP_001120916.1:p.Pro191= NP_001120916.1:p.Pro191=
platelet glycoprotein 4 isoform 1 NP_001120915.1:p.Pro191= NP_001120915.1:p.Pro191=
platelet glycoprotein 4 isoform 4 NP_001276840.1:p.Pro115= NP_001276840.1:p.Pro115=
platelet glycoprotein 4 isoform 1 NP_001358004.1:p.Pro191= NP_001358004.1:p.Pro191=
platelet glycoprotein 4 isoform 1 NP_001358006.1:p.Pro191= NP_001358006.1:p.Pro191=
platelet glycoprotein 4 isoform 6 NP_001358010.1:p.Pro36= NP_001358010.1:p.Pro36=
platelet glycoprotein 4 isoform 1 NP_001358003.1:p.Pro191= NP_001358003.1:p.Pro191=
platelet glycoprotein 4 isoform 1 NP_001358007.1:p.Pro191= NP_001358007.1:p.Pro191=
platelet glycoprotein 4 isoform 5 NP_001358008.1:p.Pro157= NP_001358008.1:p.Pro157=
platelet glycoprotein 4 isoform 2 NP_001276837.1:p.Pro191= NP_001276837.1:p.Pro191=
platelet glycoprotein 4 isoform 6 NP_001358009.1:p.Pro36= NP_001358009.1:p.Pro36=
platelet glycoprotein 4 isoform X1 XP_005250772.1:p.Pro191= XP_005250772.1:p.Pro191=
platelet glycoprotein 4 isoform X1 XP_024302771.1:p.Pro191= XP_024302771.1:p.Pro191=
platelet glycoprotein 4 isoform X1 XP_024302770.1:p.Pro191= XP_024302770.1:p.Pro191=
platelet glycoprotein 4 isoform X1 XP_047277004.1:p.Pro191= XP_047277004.1:p.Pro191=
platelet glycoprotein 4 isoform X1 XP_047277002.1:p.Pro191= XP_047277002.1:p.Pro191=
platelet glycoprotein 4 isoform X1 XP_047276997.1:p.Pro191= XP_047276997.1:p.Pro191=
platelet glycoprotein 4 isoform X1 XP_047277000.1:p.Pro191= XP_047277000.1:p.Pro191=
platelet glycoprotein 4 isoform X1 XP_047277001.1:p.Pro191= XP_047277001.1:p.Pro191=
platelet glycoprotein 4 isoform X1 XP_047276998.1:p.Pro191= XP_047276998.1:p.Pro191=
platelet glycoprotein 4 isoform X1 XP_047276999.1:p.Pro191= XP_047276999.1:p.Pro191=
platelet glycoprotein 4 isoform X1 XP_047277005.1:p.Pro191= XP_047277005.1:p.Pro191=
platelet glycoprotein 4 isoform X1 XP_047277003.1:p.Pro191= XP_047277003.1:p.Pro191=
CD36 transcript variant 7 NM_001289909.1:c.430-1273= NM_001289909.1:c.430-1273G>A
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Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

94 SubSNP, 25 Frequency, 2 ClinVar submissions
No Submitter Submission ID Date (Build)
1 WIAF-CSNP ss7566 Sep 19, 2000 (52)
2 PGA-UW-FHCRC ss4472381 May 29, 2002 (106)
3 PERLEGEN ss24517392 Sep 20, 2004 (123)
4 MGC_GENOME_DIFF ss28504618 Sep 24, 2004 (126)
5 SHGC ss66537294 Nov 30, 2006 (127)
6 SI_EXO ss71643041 May 17, 2007 (127)
7 AFFY ss74843470 Aug 16, 2007 (128)
8 ILLUMINA ss75166660 Dec 06, 2007 (129)
9 CGM_KYOTO ss76868021 Dec 06, 2007 (129)
10 CNG ss95213121 Mar 25, 2008 (129)
11 KRIBB_YJKIM ss119337730 Dec 01, 2009 (131)
12 ILLUMINA ss160752731 Dec 01, 2009 (131)
13 ILLUMINA ss173948683 Jul 04, 2010 (132)
14 1000GENOMES ss334234211 May 09, 2011 (134)
15 NHLBI-ESP ss342237932 May 09, 2011 (134)
16 ILLUMINA ss481178023 May 04, 2012 (137)
17 ILLUMINA ss481200835 May 04, 2012 (137)
18 ILLUMINA ss482188005 Sep 08, 2015 (146)
19 ILLUMINA ss485384249 May 04, 2012 (137)
20 1000GENOMES ss490947486 May 04, 2012 (137)
21 CLINSEQ_SNP ss491908718 May 04, 2012 (137)
22 ILLUMINA ss537323797 Sep 08, 2015 (146)
23 ILLUMINA ss778933017 Sep 08, 2015 (146)
24 ILLUMINA ss783137672 Sep 08, 2015 (146)
25 ILLUMINA ss784094004 Sep 08, 2015 (146)
26 ILLUMINA ss832396708 Sep 08, 2015 (146)
27 ILLUMINA ss834394617 Sep 08, 2015 (146)
28 EVA-GONL ss984456314 Aug 21, 2014 (142)
29 1000GENOMES ss1325823638 Aug 21, 2014 (142)
30 HAMMER_LAB ss1397498116 Sep 08, 2015 (146)
31 EVA_GENOME_DK ss1582273688 Apr 01, 2015 (144)
32 EVA_FINRISK ss1584053111 Apr 01, 2015 (144)
33 EVA_DECODE ss1594029733 Apr 01, 2015 (144)
34 EVA_UK10K_ALSPAC ss1618532240 Apr 01, 2015 (144)
35 EVA_UK10K_TWINSUK ss1661526273 Apr 01, 2015 (144)
36 EVA_EXAC ss1688791507 Apr 01, 2015 (144)
37 EVA_MGP ss1711169840 Apr 01, 2015 (144)
38 ILLUMINA ss1752695975 Sep 08, 2015 (146)
39 WEILL_CORNELL_DGM ss1927717751 Feb 12, 2016 (147)
40 ILLUMINA ss1959025733 Feb 12, 2016 (147)
41 JJLAB ss2024541307 Sep 14, 2016 (149)
42 USC_VALOUEV ss2152761371 Dec 20, 2016 (150)
43 HUMAN_LONGEVITY ss2295128234 Dec 20, 2016 (150)
44 ILLUMINA ss2634623259 Nov 08, 2017 (151)
45 GNOMAD ss2736521207 Nov 08, 2017 (151)
46 GNOMAD ss2747849092 Nov 08, 2017 (151)
47 GNOMAD ss2855265210 Nov 08, 2017 (151)
48 SWEGEN ss3001499915 Nov 08, 2017 (151)
49 ILLUMINA ss3022750212 Nov 08, 2017 (151)
50 ILLUMINA ss3629846987 Oct 12, 2018 (152)
51 ILLUMINA ss3632529842 Oct 12, 2018 (152)
52 ILLUMINA ss3633467711 Oct 12, 2018 (152)
53 ILLUMINA ss3634192888 Oct 12, 2018 (152)
54 ILLUMINA ss3635127099 Oct 12, 2018 (152)
55 ILLUMINA ss3635872587 Oct 12, 2018 (152)
56 ILLUMINA ss3636860328 Oct 12, 2018 (152)
57 ILLUMINA ss3637625571 Oct 12, 2018 (152)
58 ILLUMINA ss3638705753 Oct 12, 2018 (152)
59 ILLUMINA ss3640834391 Oct 12, 2018 (152)
60 ILLUMINA ss3643641043 Oct 12, 2018 (152)
61 OMUKHERJEE_ADBS ss3646358597 Oct 12, 2018 (152)
62 ILLUMINA ss3653283390 Oct 12, 2018 (152)
63 EGCUT_WGS ss3669250445 Jul 13, 2019 (153)
64 EVA_DECODE ss3720054382 Jul 13, 2019 (153)
65 ILLUMINA ss3726455790 Jul 13, 2019 (153)
66 ACPOP ss3734792329 Jul 13, 2019 (153)
67 ILLUMINA ss3745427115 Jul 13, 2019 (153)
68 PAGE_CC ss3771378538 Jul 13, 2019 (153)
69 ILLUMINA ss3772920023 Jul 13, 2019 (153)
70 EVA ss3824285928 Apr 26, 2020 (154)
71 EVA ss3825722136 Apr 26, 2020 (154)
72 SGDP_PRJ ss3867712151 Apr 26, 2020 (154)
73 KRGDB ss3914967789 Apr 26, 2020 (154)
74 EVA ss3986387027 Apr 26, 2021 (155)
75 EVA ss4017343179 Apr 26, 2021 (155)
76 TOPMED ss4751932571 Apr 26, 2021 (155)
77 TOMMO_GENOMICS ss5184071333 Apr 26, 2021 (155)
78 EVA ss5237423896 Apr 26, 2021 (155)
79 EVA ss5237649387 Oct 13, 2022 (156)
80 1000G_HIGH_COVERAGE ss5273579527 Oct 13, 2022 (156)
81 EVA ss5315258362 Oct 13, 2022 (156)
82 EVA ss5374673628 Oct 13, 2022 (156)
83 HUGCELL_USP ss5470593512 Oct 13, 2022 (156)
84 1000G_HIGH_COVERAGE ss5562109711 Oct 13, 2022 (156)
85 SANFORD_IMAGENETICS ss5624667107 Oct 13, 2022 (156)
86 SANFORD_IMAGENETICS ss5643329595 Oct 13, 2022 (156)
87 TOMMO_GENOMICS ss5724608388 Oct 13, 2022 (156)
88 EVA ss5799728540 Oct 13, 2022 (156)
89 EVA ss5823083471 Oct 13, 2022 (156)
90 EVA ss5848142476 Oct 13, 2022 (156)
91 EVA ss5848685186 Oct 13, 2022 (156)
92 EVA ss5859573118 Oct 13, 2022 (156)
93 EVA ss5972504800 Oct 13, 2022 (156)
94 EVA ss5979831315 Oct 13, 2022 (156)
95 1000Genomes NC_000007.13 - 80292449 Oct 12, 2018 (152)
96 1000Genomes_30x NC_000007.14 - 80663133 Oct 13, 2022 (156)
97 The Avon Longitudinal Study of Parents and Children NC_000007.13 - 80292449 Oct 12, 2018 (152)
98 Genome-wide autozygosity in Daghestan NC_000007.12 - 80130385 Apr 26, 2020 (154)
99 Genetic variation in the Estonian population NC_000007.13 - 80292449 Oct 12, 2018 (152)
100 ExAC NC_000007.13 - 80292449 Oct 12, 2018 (152)
101 FINRISK NC_000007.13 - 80292449 Apr 26, 2020 (154)
102 The Danish reference pan genome NC_000007.13 - 80292449 Apr 26, 2020 (154)
103 gnomAD - Genomes NC_000007.14 - 80663133 Apr 26, 2021 (155)
104 gnomAD - Exomes NC_000007.13 - 80292449 Jul 13, 2019 (153)
105 GO Exome Sequencing Project NC_000007.13 - 80292449 Oct 12, 2018 (152)
106 Genome of the Netherlands Release 5 NC_000007.13 - 80292449 Apr 26, 2020 (154)
107 HapMap NC_000007.14 - 80663133 Apr 26, 2020 (154)
108 KOREAN population from KRGDB NC_000007.13 - 80292449 Apr 26, 2020 (154)
109 Medical Genome Project healthy controls from Spanish population NC_000007.13 - 80292449 Apr 26, 2020 (154)
110 Northern Sweden NC_000007.13 - 80292449 Jul 13, 2019 (153)
111 The PAGE Study NC_000007.14 - 80663133 Jul 13, 2019 (153)
112 Qatari NC_000007.13 - 80292449 Apr 26, 2020 (154)
113 SGDP_PRJ NC_000007.13 - 80292449 Apr 26, 2020 (154)
114 Siberian NC_000007.13 - 80292449 Apr 26, 2020 (154)
115 8.3KJPN NC_000007.13 - 80292449 Apr 26, 2021 (155)
116 14KJPN NC_000007.14 - 80663133 Oct 13, 2022 (156)
117 TopMed NC_000007.14 - 80663133 Apr 26, 2021 (155)
118 UK 10K study - Twins NC_000007.13 - 80292449 Oct 12, 2018 (152)
119 ALFA NC_000007.14 - 80663133 Apr 26, 2021 (155)
120 ClinVar RCV001162667.2 Oct 13, 2022 (156)
121 ClinVar RCV001675985.2 Oct 13, 2022 (156)
Help

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID History Updated (Build)
rs3212010 Jul 03, 2002 (106)
rs17179695 Oct 08, 2004 (123)
rs17850316 Mar 11, 2006 (126)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
472255, ss481178023, ss491908718, ss1397498116, ss1594029733, ss3643641043 NC_000007.12:80130384:G:A NC_000007.14:80663132:G:A (self)
37818075, 21046441, 14988693, 8861173, 49572, 8438627, 5682862, 743885, 9397022, 22145183, 285600, 8077194, 9759681, 19729131, 5277725, 42040640, 21046441, ss334234211, ss342237932, ss481200835, ss482188005, ss485384249, ss490947486, ss537323797, ss778933017, ss783137672, ss784094004, ss832396708, ss834394617, ss984456314, ss1325823638, ss1582273688, ss1584053111, ss1618532240, ss1661526273, ss1688791507, ss1711169840, ss1752695975, ss1927717751, ss1959025733, ss2024541307, ss2152761371, ss2634623259, ss2736521207, ss2747849092, ss2855265210, ss3001499915, ss3022750212, ss3629846987, ss3632529842, ss3633467711, ss3634192888, ss3635127099, ss3635872587, ss3636860328, ss3637625571, ss3638705753, ss3640834391, ss3646358597, ss3653283390, ss3669250445, ss3734792329, ss3745427115, ss3772920023, ss3824285928, ss3825722136, ss3867712151, ss3914967789, ss3986387027, ss4017343179, ss5184071333, ss5237423896, ss5315258362, ss5374673628, ss5624667107, ss5643329595, ss5799728540, ss5823083471, ss5848142476, ss5848685186, ss5972504800, ss5979831315 NC_000007.13:80292448:G:A NC_000007.14:80663132:G:A (self)
RCV001162667.2, RCV001675985.2, 49635646, 266785054, 3428076, 600007, 58445492, 589310130, 1063597165, ss2295128234, ss3720054382, ss3726455790, ss3771378538, ss4751932571, ss5237649387, ss5273579527, ss5470593512, ss5562109711, ss5724608388, ss5859573118 NC_000007.14:80663132:G:A NC_000007.14:80663132:G:A (self)
ss7566, ss4472381, ss24517392, ss28504618, ss66537294, ss71643041, ss74843470, ss75166660, ss76868021, ss95213121, ss119337730, ss160752731, ss173948683 NT_007933.15:18325291:G:A NC_000007.14:80663132:G:A (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

5 citations for rs5956
PMID Title Author Year Journal
23856131 Is CD36 gene polymorphism in region encoding lipid-binding domain associated with early onset CAD? Rać M et al. 2013 Gene
24049523 Association of CD36 gene polymorphisms with echo- and electrocardiographic parameters in patients with early onset coronary artery disease. Rac M et al. 2013 Archives of medical science
25118627 Associations between CD36 gene polymorphisms and susceptibility to coronary artery heart disease. Zhang Y et al. 2014 Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas
25916834 Is plasma soluble CD36 associated with cardiovascular risk factors in early onset coronary artery disease patients? Krzystolik A et al. 2015 Scandinavian journal of clinical and laboratory investigation
27461004 Association of six CpG-SNPs in the inflammation-related genes with coronary heart disease. Chen X et al. 2016 Human genomics
Help

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:
Select flank length:

Genomic regions, transcripts, and products
Top▲ Help

NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 2.0.1.post761+d5e8e07