Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

dbSNP Short Genetic Variations

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.

rs590787

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr1:25303452 (GRCh38.p13) 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
A>C / A>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.000074 (9/120834, GnomAD)
C=0.23708 (9756/41150, ALFA)
C=0.00102 (17/16668, 8.3KJPN) (+ 5 more)
C=0.1244 (623/5008, 1000G)
C=0.0131 (24/1832, Korea1K)
G=0.217 (63/290, HapMap)
A=0.5 (1/2, Siberian)
C=0.5 (1/2, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
RHD : Missense Variant
RSRP1 : Non Coding Transcript Variant
Publications
1 citation
Genomic View
See rs on genome
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.p13 chr 1 NC_000001.11:g.25303452A>C
GRCh38.p13 chr 1 NC_000001.11:g.25303452A>G
GRCh37.p13 chr 1 NC_000001.10:g.25629943A>C
GRCh37.p13 chr 1 NC_000001.10:g.25629943A>G
RHD RefSeqGene (LRG_796) NG_007494.1:g.35963A>C
RHD RefSeqGene (LRG_796) NG_007494.1:g.35963A>G
Gene: RSRP1, arginine and serine rich protein 1 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
RSRP1 transcript variant 14 NM_001321772.2:c.-67+3358…

NM_001321772.2:c.-67+33588T>G

N/A Intron Variant
RSRP1 transcript variant 2 NM_020317.5:c. N/A Genic Upstream Transcript Variant
RSRP1 transcript variant 18 NR_135790.1:n.2794T>G N/A Non Coding Transcript Variant
RSRP1 transcript variant 18 NR_135790.1:n.2794T>C N/A Non Coding Transcript Variant
RSRP1 transcript variant 20 NR_135792.1:n.2585T>G N/A Non Coding Transcript Variant
RSRP1 transcript variant 20 NR_135792.1:n.2585T>C N/A Non Coding Transcript Variant
RSRP1 transcript variant 19 NR_135791.1:n.2973T>G N/A Non Coding Transcript Variant
RSRP1 transcript variant 19 NR_135791.1:n.2973T>C N/A Non Coding Transcript Variant
RSRP1 transcript variant 21 NR_135793.1:n.2639T>G N/A Non Coding Transcript Variant
RSRP1 transcript variant 21 NR_135793.1:n.2639T>C N/A Non Coding Transcript Variant
RSRP1 transcript variant 15 NR_135787.2:n. N/A Intron Variant
RSRP1 transcript variant 16 NR_135788.2:n. N/A Intron Variant
RSRP1 transcript variant 17 NR_135789.2:n. N/A Intron Variant
RSRP1 transcript variant 3 NR_135143.2:n. N/A Genic Upstream Transcript Variant
RSRP1 transcript variant 4 NR_135144.2:n. N/A Genic Upstream Transcript Variant
RSRP1 transcript variant 5 NR_135777.2:n. N/A Genic Upstream Transcript Variant
RSRP1 transcript variant 6 NR_135778.2:n. N/A Genic Upstream Transcript Variant
RSRP1 transcript variant 7 NR_135780.2:n. N/A Genic Upstream Transcript Variant
RSRP1 transcript variant 8 NR_135781.2:n. N/A Genic Upstream Transcript Variant
RSRP1 transcript variant 9 NR_135782.2:n. N/A Genic Upstream Transcript Variant
RSRP1 transcript variant 10 NR_135783.2:n. N/A Genic Upstream Transcript Variant
RSRP1 transcript variant 11 NR_135784.2:n. N/A Genic Upstream Transcript Variant
RSRP1 transcript variant 12 NR_135785.2:n. N/A Genic Upstream Transcript Variant
RSRP1 transcript variant 13 NR_135786.2:n. N/A Genic Upstream Transcript Variant
RSRP1 transcript variant X1 XM_011541797.1:c. N/A Genic Upstream Transcript Variant
RSRP1 transcript variant X2 XR_946709.2:n. N/A Genic Upstream Transcript Variant
Gene: RHD, Rh blood group D antigen (plus strand)
Molecule type Change Amino acid[Codon] SO Term
RHD transcript variant 3 NM_001282867.1:c.434A>C Y [TAC] > S [TCC] Coding Sequence Variant
blood group Rh(D) polypeptide isoform 3 NP_001269796.1:p.Tyr145Ser Y (Tyr) > S (Ser) Missense Variant
RHD transcript variant 3 NM_001282867.1:c.434A>G Y [TAC] > C [TGC] Coding Sequence Variant
blood group Rh(D) polypeptide isoform 3 NP_001269796.1:p.Tyr145Cys Y (Tyr) > C (Cys) Missense Variant
RHD transcript variant 4 NM_001282868.1:c.932A>C Y [TAC] > S [TCC] Coding Sequence Variant
blood group Rh(D) polypeptide isoform 4 NP_001269797.1:p.Tyr311Ser Y (Tyr) > S (Ser) Missense Variant
RHD transcript variant 4 NM_001282868.1:c.932A>G Y [TAC] > C [TGC] Coding Sequence Variant
blood group Rh(D) polypeptide isoform 4 NP_001269797.1:p.Tyr311Cys Y (Tyr) > C (Cys) Missense Variant
RHD transcript variant 6 NM_001282870.1:c.932A>C Y [TAC] > S [TCC] Coding Sequence Variant
blood group Rh(D) polypeptide isoform 6 NP_001269799.1:p.Tyr311Ser Y (Tyr) > S (Ser) Missense Variant
RHD transcript variant 6 NM_001282870.1:c.932A>G Y [TAC] > C [TGC] Coding Sequence Variant
blood group Rh(D) polypeptide isoform 6 NP_001269799.1:p.Tyr311Cys Y (Tyr) > C (Cys) Missense Variant
RHD transcript variant 8 NM_001282872.1:c.932A>C Y [TAC] > S [TCC] Coding Sequence Variant
blood group Rh(D) polypeptide isoform 8 NP_001269801.1:p.Tyr311Ser Y (Tyr) > S (Ser) Missense Variant
RHD transcript variant 8 NM_001282872.1:c.932A>G Y [TAC] > C [TGC] Coding Sequence Variant
blood group Rh(D) polypeptide isoform 8 NP_001269801.1:p.Tyr311Cys Y (Tyr) > C (Cys) Missense Variant
RHD transcript variant 2 NM_001127691.3:c.932A>C Y [TAC] > S [TCC] Coding Sequence Variant
blood group Rh(D) polypeptide isoform 2 NP_001121163.1:p.Tyr311Ser Y (Tyr) > S (Ser) Missense Variant
RHD transcript variant 2 NM_001127691.3:c.932A>G Y [TAC] > C [TGC] Coding Sequence Variant
blood group Rh(D) polypeptide isoform 2 NP_001121163.1:p.Tyr311Cys Y (Tyr) > C (Cys) Missense Variant
RHD transcript variant 5 NM_001282869.2:c.932A>C Y [TAC] > S [TCC] Coding Sequence Variant
blood group Rh(D) polypeptide isoform 5 NP_001269798.1:p.Tyr311Ser Y (Tyr) > S (Ser) Missense Variant
RHD transcript variant 5 NM_001282869.2:c.932A>G Y [TAC] > C [TGC] Coding Sequence Variant
blood group Rh(D) polypeptide isoform 5 NP_001269798.1:p.Tyr311Cys Y (Tyr) > C (Cys) Missense Variant
RHD transcript variant 7 NM_001282871.2:c.932A>C Y [TAC] > S [TCC] Coding Sequence Variant
blood group Rh(D) polypeptide isoform 7 NP_001269800.1:p.Tyr311Ser Y (Tyr) > S (Ser) Missense Variant
RHD transcript variant 7 NM_001282871.2:c.932A>G Y [TAC] > C [TGC] Coding Sequence Variant
blood group Rh(D) polypeptide isoform 7 NP_001269800.1:p.Tyr311Cys Y (Tyr) > C (Cys) Missense Variant
RHD transcript variant 1 NM_016124.5:c.932A>C Y [TAC] > S [TCC] Coding Sequence Variant
blood group Rh(D) polypeptide isoform 1 NP_057208.2:p.Tyr311Ser Y (Tyr) > S (Ser) Missense Variant
RHD transcript variant 1 NM_016124.5:c.932A>G Y [TAC] > C [TGC] Coding Sequence Variant
blood group Rh(D) polypeptide isoform 1 NP_057208.2:p.Tyr311Cys Y (Tyr) > C (Cys) Missense Variant
RHD transcript variant X1 XM_017002015.1:c.932A>C Y [TAC] > S [TCC] Coding Sequence Variant
blood group Rh(D) polypeptide isoform X1 XP_016857504.1:p.Tyr311Ser Y (Tyr) > S (Ser) Missense Variant
RHD transcript variant X1 XM_017002015.1:c.932A>G Y [TAC] > C [TGC] Coding Sequence Variant
blood group Rh(D) polypeptide isoform X1 XP_016857504.1:p.Tyr311Cys Y (Tyr) > C (Cys) Missense Variant
RHD transcript variant X2 XR_946736.1:n.1087A>C N/A Non Coding Transcript Variant
RHD transcript variant X2 XR_946736.1:n.1087A>G N/A Non Coding Transcript Variant
RHD transcript variant X3 XR_946737.2:n.1087A>C N/A Non Coding Transcript Variant
RHD transcript variant X3 XR_946737.2:n.1087A>G N/A Non Coding Transcript 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.

Not Reported in ClinVar

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: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 41150 A=0.76287 C=0.23708, G=0.00005
European Sub 30138 A=0.70098 C=0.29899, G=0.00003
African Sub 2920 A=0.9894 C=0.0106, G=0.0000
African Others Sub 108 A=1.000 C=0.000, G=0.000
African American Sub 2812 A=0.9890 C=0.0110, G=0.0000
Asian Sub 3006 A=0.9987 C=0.0013, G=0.0000
East Asian Sub 1826 A=0.9984 C=0.0016, G=0.0000
Other Asian Sub 1180 A=0.9992 C=0.0008, G=0.0000
Latin American 1 Sub 152 A=0.980 C=0.020, G=0.000
Latin American 2 Sub 612 A=1.000 C=0.000, G=0.000
South Asian Sub 94 A=1.00 C=0.00, G=0.00
Other Sub 4228 A=0.8325 C=0.1672, G=0.0002


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
gnomAD - Genomes Global Study-wide 120834 A=0.999926 G=0.000074
gnomAD - Genomes European Sub 62030 A=0.99990 G=0.00010
gnomAD - Genomes African Sub 38702 A=0.99992 G=0.00008
gnomAD - Genomes American Sub 12214 A=1.00000 G=0.00000
gnomAD - Genomes East Asian Sub 3100 A=1.0000 G=0.0000
gnomAD - Genomes Ashkenazi Jewish Sub 2948 A=1.0000 G=0.0000
gnomAD - Genomes Other Sub 1840 A=1.0000 G=0.0000
8.3KJPN JAPANESE Study-wide 16668 A=0.99898 C=0.00102
1000Genomes Global Study-wide 5008 A=0.8756 C=0.1244
1000Genomes African Sub 1322 A=0.9448 C=0.0552
1000Genomes East Asian Sub 1008 A=0.7192 C=0.2808
1000Genomes Europe Sub 1006 A=0.8390 C=0.1610
1000Genomes South Asian Sub 978 A=0.983 C=0.017
1000Genomes American Sub 694 A=0.873 C=0.127
Korean Genome Project KOREAN Study-wide 1832 A=0.9869 C=0.0131
HapMap Global Study-wide 290 A=0.783 G=0.217
HapMap African Sub 108 A=0.796 G=0.204
HapMap American Sub 96 A=0.61 G=0.39
HapMap Asian Sub 86 A=0.95 G=0.05
Siberian Global Study-wide 2 A=0.5 C=0.5
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 A= C G
GRCh38.p13 chr 1 NC_000001.11:g.25303452= NC_000001.11:g.25303452A>C NC_000001.11:g.25303452A>G
GRCh37.p13 chr 1 NC_000001.10:g.25629943= NC_000001.10:g.25629943A>C NC_000001.10:g.25629943A>G
RHD RefSeqGene (LRG_796) NG_007494.1:g.35963= NG_007494.1:g.35963A>C NG_007494.1:g.35963A>G
RHD transcript variant 1 NM_016124.4:c.932= NM_016124.4:c.932A>C NM_016124.4:c.932A>G
RHD transcript variant 1 NM_016124.5:c.932= NM_016124.5:c.932A>C NM_016124.5:c.932A>G
RHD transcript variant 1 NM_016124.3:c.932= NM_016124.3:c.932A>C NM_016124.3:c.932A>G
RHD transcript variant 2 NM_001127691.3:c.932= NM_001127691.3:c.932A>C NM_001127691.3:c.932A>G
RHD transcript variant 2 NM_001127691.2:c.932= NM_001127691.2:c.932A>C NM_001127691.2:c.932A>G
RHD transcript variant 2 NM_001127691.1:c.932= NM_001127691.1:c.932A>C NM_001127691.1:c.932A>G
RHD transcript variant 7 NM_001282871.2:c.932= NM_001282871.2:c.932A>C NM_001282871.2:c.932A>G
RHD transcript variant 7 NM_001282871.1:c.932= NM_001282871.1:c.932A>C NM_001282871.1:c.932A>G
RHD transcript variant 5 NM_001282869.2:c.932= NM_001282869.2:c.932A>C NM_001282869.2:c.932A>G
RHD transcript variant 5 NM_001282869.1:c.932= NM_001282869.1:c.932A>C NM_001282869.1:c.932A>G
RHD transcript variant 8 NM_001282872.1:c.932= NM_001282872.1:c.932A>C NM_001282872.1:c.932A>G
RHD transcript variant 3 NM_001282867.1:c.434= NM_001282867.1:c.434A>C NM_001282867.1:c.434A>G
RHD transcript variant 6 NM_001282870.1:c.932= NM_001282870.1:c.932A>C NM_001282870.1:c.932A>G
RHD transcript variant 4 NM_001282868.1:c.932= NM_001282868.1:c.932A>C NM_001282868.1:c.932A>G
RHD transcript variant 2 NM_016225.3:c.932= NM_016225.3:c.932A>C NM_016225.3:c.932A>G
RHD transcript variant 2 NM_016225.2:c.932= NM_016225.2:c.932A>C NM_016225.2:c.932A>G
RHD transcript variant X3 XR_946737.2:n.1087= XR_946737.2:n.1087A>C XR_946737.2:n.1087A>G
RSRP1 transcript variant 19 NR_135791.1:n.2973= NR_135791.1:n.2973T>G NR_135791.1:n.2973T>C
RSRP1 transcript variant 18 NR_135790.1:n.2794= NR_135790.1:n.2794T>G NR_135790.1:n.2794T>C
RSRP1 transcript variant 21 NR_135793.1:n.2639= NR_135793.1:n.2639T>G NR_135793.1:n.2639T>C
RSRP1 transcript variant 20 NR_135792.1:n.2585= NR_135792.1:n.2585T>G NR_135792.1:n.2585T>C
RHD transcript variant X1 XM_017002015.1:c.932= XM_017002015.1:c.932A>C XM_017002015.1:c.932A>G
RHD transcript variant X2 XR_946736.1:n.1087= XR_946736.1:n.1087A>C XR_946736.1:n.1087A>G
LOC51698 transcript NM_016225.1:c.932= NM_016225.1:c.932A>C NM_016225.1:c.932A>G
blood group Rh(D) polypeptide isoform 1 NP_057208.2:p.Tyr311= NP_057208.2:p.Tyr311Ser NP_057208.2:p.Tyr311Cys
blood group Rh(D) polypeptide isoform 2 NP_001121163.1:p.Tyr311= NP_001121163.1:p.Tyr311Ser NP_001121163.1:p.Tyr311Cys
blood group Rh(D) polypeptide isoform 7 NP_001269800.1:p.Tyr311= NP_001269800.1:p.Tyr311Ser NP_001269800.1:p.Tyr311Cys
blood group Rh(D) polypeptide isoform 5 NP_001269798.1:p.Tyr311= NP_001269798.1:p.Tyr311Ser NP_001269798.1:p.Tyr311Cys
blood group Rh(D) polypeptide isoform 8 NP_001269801.1:p.Tyr311= NP_001269801.1:p.Tyr311Ser NP_001269801.1:p.Tyr311Cys
blood group Rh(D) polypeptide isoform 3 NP_001269796.1:p.Tyr145= NP_001269796.1:p.Tyr145Ser NP_001269796.1:p.Tyr145Cys
blood group Rh(D) polypeptide isoform 6 NP_001269799.1:p.Tyr311= NP_001269799.1:p.Tyr311Ser NP_001269799.1:p.Tyr311Cys
blood group Rh(D) polypeptide isoform 4 NP_001269797.1:p.Tyr311= NP_001269797.1:p.Tyr311Ser NP_001269797.1:p.Tyr311Cys
blood group Rh(D) polypeptide isoform X1 XP_016857504.1:p.Tyr311= XP_016857504.1:p.Tyr311Ser XP_016857504.1:p.Tyr311Cys
RSRP1 transcript variant 14 NM_001321772.2:c.-67+33588= NM_001321772.2:c.-67+33588T>G NM_001321772.2:c.-67+33588T>C
RHD transcript variant X6 XM_005245964.1:c.487-3144= XM_005245964.1:c.487-3144A>C XM_005245964.1:c.487-3144A>G
Help

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#.

32 SubSNP, 11 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss2862759 Jan 23, 2001 (94)
2 SEQUENOM ss24796070 Sep 20, 2004 (123)
3 SI_EXO ss76897022 Dec 06, 2007 (129)
4 EXOME_CHIP ss491289448 May 04, 2012 (137)
5 TISHKOFF ss553907207 Apr 25, 2013 (138)
6 ILLUMINA ss783452562 Sep 08, 2015 (146)
7 1000GENOMES ss1290089479 Aug 21, 2014 (142)
8 EVA_EXAC ss1685398899 Apr 01, 2015 (144)
9 EVA_EXAC ss1685398900 Apr 01, 2015 (144)
10 ILLUMINA ss1751912853 Sep 08, 2015 (146)
11 ILLUMINA ss1917725008 Feb 12, 2016 (147)
12 ILLUMINA ss1945988623 Feb 12, 2016 (147)
13 ILLUMINA ss1958254327 Feb 12, 2016 (147)
14 USC_VALOUEV ss2147604189 Dec 20, 2016 (150)
15 GRF ss2697509815 Nov 08, 2017 (151)
16 GNOMAD ss2731264926 Nov 08, 2017 (151)
17 GNOMAD ss2746262165 Nov 08, 2017 (151)
18 GNOMAD ss2752823159 Nov 08, 2017 (151)
19 AFFY ss2984850853 Nov 08, 2017 (151)
20 ILLUMINA ss3021067986 Nov 08, 2017 (151)
21 TOPMED ss3071294468 Nov 08, 2017 (151)
22 ILLUMINA ss3634313463 Oct 11, 2018 (152)
23 ILLUMINA ss3640020827 Oct 11, 2018 (152)
24 ILLUMINA ss3651393406 Oct 11, 2018 (152)
25 ILLUMINA ss3653623922 Oct 11, 2018 (152)
26 ILLUMINA ss3744341770 Jul 12, 2019 (153)
27 ILLUMINA ss3744614419 Jul 12, 2019 (153)
28 ILLUMINA ss3772115972 Jul 12, 2019 (153)
29 KHV_HUMAN_GENOMES ss3798977491 Jul 12, 2019 (153)
30 KOGIC ss3944066781 Apr 25, 2020 (154)
31 EVA ss3986009781 Apr 25, 2021 (155)
32 TOMMO_GENOMICS ss5142995936 Apr 25, 2021 (155)
33 1000Genomes NC_000001.10 - 25629943 Oct 11, 2018 (152)
34 ExAC

Submission ignored due to conflicting rows:
Row 4584610 (NC_000001.10:25629942:A:A 98068/99698, NC_000001.10:25629942:A:C 1630/99698)
Row 4584611 (NC_000001.10:25629942:A:A 99683/99698, NC_000001.10:25629942:A:G 15/99698)

- Oct 11, 2018 (152)
35 ExAC

Submission ignored due to conflicting rows:
Row 4584610 (NC_000001.10:25629942:A:A 98068/99698, NC_000001.10:25629942:A:C 1630/99698)
Row 4584611 (NC_000001.10:25629942:A:A 99683/99698, NC_000001.10:25629942:A:G 15/99698)

- Oct 11, 2018 (152)
36 gnomAD - Genomes NC_000001.11 - 25303452 Apr 25, 2021 (155)
37 gnomAD - Exomes

Submission ignored due to conflicting rows:
Row 278868 (NC_000001.10:25629942:A:A 218008/219088, NC_000001.10:25629942:A:C 1080/219088)
Row 278869 (NC_000001.10:25629942:A:A 219069/219088, NC_000001.10:25629942:A:G 19/219088)

- Jul 12, 2019 (153)
38 gnomAD - Exomes

Submission ignored due to conflicting rows:
Row 278868 (NC_000001.10:25629942:A:A 218008/219088, NC_000001.10:25629942:A:C 1080/219088)
Row 278869 (NC_000001.10:25629942:A:A 219069/219088, NC_000001.10:25629942:A:G 19/219088)

- Jul 12, 2019 (153)
39 HapMap NC_000001.11 - 25303452 Apr 25, 2020 (154)
40 Korean Genome Project NC_000001.11 - 25303452 Apr 25, 2020 (154)
41 Siberian NC_000001.10 - 25629943 Apr 25, 2020 (154)
42 8.3KJPN NC_000001.10 - 25629943 Apr 25, 2021 (155)
43 ALFA NC_000001.11 - 25303452 Apr 25, 2021 (155)
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)
rs2020161 Apr 12, 2001 (94)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
779454, 120543, 965243, ss491289448, ss783452562, ss1290089479, ss1685398899, ss1751912853, ss1917725008, ss1945988623, ss1958254327, ss2147604189, ss2697509815, ss2731264926, ss2984850853, ss3021067986, ss3634313463, ss3640020827, ss3651393406, ss3653623922, ss3744341770, ss3744614419, ss3772115972, ss3986009781, ss5142995936 NC_000001.10:25629942:A:C NC_000001.11:25303451:A:C (self)
444782, 13490708964, ss3798977491, ss3944066781 NC_000001.11:25303451:A:C NC_000001.11:25303451:A:C (self)
ss553907207, ss1685398900, ss2731264926, ss2746262165, ss2752823159 NC_000001.10:25629942:A:G NC_000001.11:25303451:A:G (self)
5449184, 32574, 13490708964, ss3071294468 NC_000001.11:25303451:A:G NC_000001.11:25303451:A:G (self)
ss76897022 NT_004610.18:8454284:A:G NC_000001.11:25303451:A:G (self)
ss2862759, ss24796070 NT_004610.19:12310030:A:G NC_000001.11:25303451:A:G (self)
Help

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

1 citation for rs590787
PMID Title Author Year Journal
30950221 Effects of RHD gene polymorphisms on distinguishing weak D or DEL from RhD- in blood donation in a Chinese population. Shi J et al. 2019 Molecular genetics & genomic medicine
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.post596+ae089ad