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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.

rs150102121

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr20:54169599 (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
C>G / C>T
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.00006 (2/35428, ALFA)
T=0.00008 (1/13006, GO-ESP)
G=0.0006 (4/6404, 1000G_30x) (+ 1 more)
G=0.0006 (3/5008, 1000G)
Clinical Significance
Reported in ClinVar
Gene : Consequence
CYP24A1 : Synonymous Variant
Publications
0 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 35428 C=0.99994 G=0.00000, T=0.00006
European Sub 26588 C=0.99992 G=0.00000, T=0.00008
African Sub 2918 C=1.0000 G=0.0000, T=0.0000
African Others Sub 114 C=1.000 G=0.000, T=0.000
African American Sub 2804 C=1.0000 G=0.0000, T=0.0000
Asian Sub 112 C=1.000 G=0.000, T=0.000
East Asian Sub 86 C=1.00 G=0.00, T=0.00
Other Asian Sub 26 C=1.00 G=0.00, T=0.00
Latin American 1 Sub 500 C=1.000 G=0.000, T=0.000
Latin American 2 Sub 624 C=1.000 G=0.000, T=0.000
South Asian Sub 98 C=1.00 G=0.00, T=0.00
Other Sub 4588 C=1.0000 G=0.0000, T=0.0000


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
Allele Frequency Aggregator Total Global 35428 C=0.99994 G=0.00000, T=0.00006
Allele Frequency Aggregator European Sub 26588 C=0.99992 G=0.00000, T=0.00008
Allele Frequency Aggregator Other Sub 4588 C=1.0000 G=0.0000, T=0.0000
Allele Frequency Aggregator African Sub 2918 C=1.0000 G=0.0000, T=0.0000
Allele Frequency Aggregator Latin American 2 Sub 624 C=1.000 G=0.000, T=0.000
Allele Frequency Aggregator Latin American 1 Sub 500 C=1.000 G=0.000, T=0.000
Allele Frequency Aggregator Asian Sub 112 C=1.000 G=0.000, T=0.000
Allele Frequency Aggregator South Asian Sub 98 C=1.00 G=0.00, T=0.00
GO Exome Sequencing Project Global Study-wide 13006 C=0.99992 T=0.00008
GO Exome Sequencing Project European American Sub 8600 C=0.9999 T=0.0001
GO Exome Sequencing Project African American Sub 4406 C=1.0000 T=0.0000
1000Genomes_30x Global Study-wide 6404 C=0.9991 G=0.0006, T=0.0003
1000Genomes_30x African Sub 1786 C=0.9989 G=0.0011, T=0.0000
1000Genomes_30x Europe Sub 1266 C=1.0000 G=0.0000, T=0.0000
1000Genomes_30x South Asian Sub 1202 C=0.9992 G=0.0000, T=0.0008
1000Genomes_30x East Asian Sub 1170 C=0.9991 G=0.0000, T=0.0009
1000Genomes_30x American Sub 980 C=0.998 G=0.002, T=0.000
1000Genomes Global Study-wide 5008 C=0.9994 G=0.0006
1000Genomes African Sub 1322 C=0.9992 G=0.0008
1000Genomes East Asian Sub 1008 C=1.0000 G=0.0000
1000Genomes Europe Sub 1006 C=1.0000 G=0.0000
1000Genomes South Asian Sub 978 C=1.000 G=0.000
1000Genomes American Sub 694 C=0.997 G=0.003
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 20 NC_000020.11:g.54169599C>G
GRCh38.p14 chr 20 NC_000020.11:g.54169599C>T
GRCh37.p13 chr 20 NC_000020.10:g.52786138C>G
GRCh37.p13 chr 20 NC_000020.10:g.52786138C>T
CYP24A1 RefSeqGene NG_008334.1:g.9379G>C
CYP24A1 RefSeqGene NG_008334.1:g.9379G>A
Gene: CYP24A1, cytochrome P450 family 24 subfamily A member 1 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
CYP24A1 transcript variant 1 NM_000782.5:c.633G>C S [TCG] > S [TCC] Coding Sequence Variant
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform 1 precursor NP_000773.2:p.Ser211= S (Ser) > S (Ser) Synonymous Variant
CYP24A1 transcript variant 1 NM_000782.5:c.633G>A S [TCG] > S [TCA] Coding Sequence Variant
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform 1 precursor NP_000773.2:p.Ser211= S (Ser) > S (Ser) Synonymous Variant
CYP24A1 transcript variant 2 NM_001128915.2:c.633G>C S [TCG] > S [TCC] Coding Sequence Variant
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform 2 precursor NP_001122387.1:p.Ser211= S (Ser) > S (Ser) Synonymous Variant
CYP24A1 transcript variant 2 NM_001128915.2:c.633G>A S [TCG] > S [TCA] Coding Sequence Variant
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform 2 precursor NP_001122387.1:p.Ser211= S (Ser) > S (Ser) Synonymous Variant
CYP24A1 transcript variant X1 XM_005260304.6:c.633G>C S [TCG] > S [TCC] Coding Sequence Variant
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X1 XP_005260361.1:p.Ser211= S (Ser) > S (Ser) Synonymous Variant
CYP24A1 transcript variant X1 XM_005260304.6:c.633G>A S [TCG] > S [TCA] Coding Sequence Variant
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X1 XP_005260361.1:p.Ser211= S (Ser) > S (Ser) Synonymous Variant
CYP24A1 transcript variant X2 XM_017027691.3:c.633G>C S [TCG] > S [TCC] Coding Sequence Variant
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X1 XP_016883180.1:p.Ser211= S (Ser) > S (Ser) Synonymous Variant
CYP24A1 transcript variant X2 XM_017027691.3:c.633G>A S [TCG] > S [TCA] Coding Sequence Variant
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X1 XP_016883180.1:p.Ser211= S (Ser) > S (Ser) Synonymous Variant
CYP24A1 transcript variant X3 XM_017027692.3:c.633G>C S [TCG] > S [TCC] Coding Sequence Variant
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X1 XP_016883181.1:p.Ser211= S (Ser) > S (Ser) Synonymous Variant
CYP24A1 transcript variant X3 XM_017027692.3:c.633G>A S [TCG] > S [TCA] Coding Sequence Variant
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X1 XP_016883181.1:p.Ser211= S (Ser) > S (Ser) Synonymous Variant
CYP24A1 transcript variant X4 XM_047439936.1:c.633G>C S [TCG] > S [TCC] Coding Sequence Variant
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X2 XP_047295892.1:p.Ser211= S (Ser) > S (Ser) Synonymous Variant
CYP24A1 transcript variant X4 XM_047439936.1:c.633G>A S [TCG] > S [TCA] Coding Sequence Variant
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X2 XP_047295892.1:p.Ser211= S (Ser) > S (Ser) Synonymous Variant
CYP24A1 transcript variant X5 XM_017027693.3:c.633G>C S [TCG] > S [TCC] Coding Sequence Variant
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X2 XP_016883182.1:p.Ser211= S (Ser) > S (Ser) Synonymous Variant
CYP24A1 transcript variant X5 XM_017027693.3:c.633G>A S [TCG] > S [TCA] Coding Sequence Variant
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X2 XP_016883182.1:p.Ser211= S (Ser) > S (Ser) Synonymous Variant
CYP24A1 transcript variant X6 XM_047439937.1:c.633G>C S [TCG] > S [TCC] Coding Sequence Variant
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X2 XP_047295893.1:p.Ser211= S (Ser) > S (Ser) Synonymous Variant
CYP24A1 transcript variant X6 XM_047439937.1:c.633G>A S [TCG] > S [TCA] Coding Sequence Variant
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X2 XP_047295893.1:p.Ser211= S (Ser) > S (Ser) Synonymous Variant
CYP24A1 transcript variant X7 XM_047439938.1:c.633G>C S [TCG] > S [TCC] Coding Sequence Variant
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X2 XP_047295894.1:p.Ser211= S (Ser) > S (Ser) Synonymous Variant
CYP24A1 transcript variant X7 XM_047439938.1:c.633G>A S [TCG] > S [TCA] Coding Sequence Variant
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X2 XP_047295894.1:p.Ser211= S (Ser) > S (Ser) 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: T (allele ID: 694569 )
ClinVar Accession Disease Names Clinical Significance
RCV000871491.3 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 C= G T
GRCh38.p14 chr 20 NC_000020.11:g.54169599= NC_000020.11:g.54169599C>G NC_000020.11:g.54169599C>T
GRCh37.p13 chr 20 NC_000020.10:g.52786138= NC_000020.10:g.52786138C>G NC_000020.10:g.52786138C>T
CYP24A1 RefSeqGene NG_008334.1:g.9379= NG_008334.1:g.9379G>C NG_008334.1:g.9379G>A
CYP24A1 transcript variant 1 NM_000782.5:c.633= NM_000782.5:c.633G>C NM_000782.5:c.633G>A
CYP24A1 transcript variant 1 NM_000782.4:c.633= NM_000782.4:c.633G>C NM_000782.4:c.633G>A
CYP24A1 transcript variant 2 NM_001128915.2:c.633= NM_001128915.2:c.633G>C NM_001128915.2:c.633G>A
CYP24A1 transcript variant 2 NM_001128915.1:c.633= NM_001128915.1:c.633G>C NM_001128915.1:c.633G>A
CYP24A1 transcript variant X1 XM_005260304.6:c.633= XM_005260304.6:c.633G>C XM_005260304.6:c.633G>A
CYP24A1 transcript variant X1 XM_005260304.5:c.633= XM_005260304.5:c.633G>C XM_005260304.5:c.633G>A
CYP24A1 transcript variant X1 XM_005260304.4:c.633= XM_005260304.4:c.633G>C XM_005260304.4:c.633G>A
CYP24A1 transcript variant X1 XM_005260304.3:c.633= XM_005260304.3:c.633G>C XM_005260304.3:c.633G>A
CYP24A1 transcript variant X1 XM_005260304.2:c.633= XM_005260304.2:c.633G>C XM_005260304.2:c.633G>A
CYP24A1 transcript variant X1 XM_005260304.1:c.633= XM_005260304.1:c.633G>C XM_005260304.1:c.633G>A
CYP24A1 transcript variant X3 XM_017027692.3:c.633= XM_017027692.3:c.633G>C XM_017027692.3:c.633G>A
CYP24A1 transcript variant X3 XM_017027692.2:c.633= XM_017027692.2:c.633G>C XM_017027692.2:c.633G>A
CYP24A1 transcript variant X3 XM_017027692.1:c.633= XM_017027692.1:c.633G>C XM_017027692.1:c.633G>A
CYP24A1 transcript variant X2 XM_017027691.3:c.633= XM_017027691.3:c.633G>C XM_017027691.3:c.633G>A
CYP24A1 transcript variant X2 XM_017027691.2:c.633= XM_017027691.2:c.633G>C XM_017027691.2:c.633G>A
CYP24A1 transcript variant X2 XM_017027691.1:c.633= XM_017027691.1:c.633G>C XM_017027691.1:c.633G>A
CYP24A1 transcript variant X5 XM_017027693.3:c.633= XM_017027693.3:c.633G>C XM_017027693.3:c.633G>A
CYP24A1 transcript variant X4 XM_017027693.2:c.633= XM_017027693.2:c.633G>C XM_017027693.2:c.633G>A
CYP24A1 transcript variant X4 XM_017027693.1:c.633= XM_017027693.1:c.633G>C XM_017027693.1:c.633G>A
CYP24A1 transcript variant X4 XM_047439936.1:c.633= XM_047439936.1:c.633G>C XM_047439936.1:c.633G>A
CYP24A1 transcript variant X7 XM_047439938.1:c.633= XM_047439938.1:c.633G>C XM_047439938.1:c.633G>A
CYP24A1 transcript variant X6 XM_047439937.1:c.633= XM_047439937.1:c.633G>C XM_047439937.1:c.633G>A
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform 1 precursor NP_000773.2:p.Ser211= NP_000773.2:p.Ser211= NP_000773.2:p.Ser211=
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform 2 precursor NP_001122387.1:p.Ser211= NP_001122387.1:p.Ser211= NP_001122387.1:p.Ser211=
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X1 XP_005260361.1:p.Ser211= XP_005260361.1:p.Ser211= XP_005260361.1:p.Ser211=
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X1 XP_016883181.1:p.Ser211= XP_016883181.1:p.Ser211= XP_016883181.1:p.Ser211=
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X1 XP_016883180.1:p.Ser211= XP_016883180.1:p.Ser211= XP_016883180.1:p.Ser211=
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X2 XP_016883182.1:p.Ser211= XP_016883182.1:p.Ser211= XP_016883182.1:p.Ser211=
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X2 XP_047295892.1:p.Ser211= XP_047295892.1:p.Ser211= XP_047295892.1:p.Ser211=
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X2 XP_047295894.1:p.Ser211= XP_047295894.1:p.Ser211= XP_047295894.1:p.Ser211=
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial isoform X2 XP_047295893.1:p.Ser211= XP_047295893.1:p.Ser211= XP_047295893.1:p.Ser211=
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#.

19 SubSNP, 12 Frequency, 1 ClinVar submissions
No Submitter Submission ID Date (Build)
1 NHLBI-ESP ss342525570 May 09, 2011 (134)
2 1000GENOMES ss1365188341 Aug 21, 2014 (142)
3 EVA_EXAC ss1694048337 Apr 01, 2015 (144)
4 EVA_EXAC ss1694048338 Apr 01, 2015 (144)
5 EVA_DECODE ss1698891287 Apr 01, 2015 (144)
6 HUMAN_LONGEVITY ss2243611363 Dec 20, 2016 (150)
7 GNOMAD ss2744685947 Nov 08, 2017 (151)
8 GNOMAD ss2750406124 Nov 08, 2017 (151)
9 GNOMAD ss2968604548 Nov 08, 2017 (151)
10 EVA_DECODE ss3707158714 Jul 13, 2019 (153)
11 EVA ss3825382950 Apr 27, 2020 (154)
12 TOPMED ss5092213281 Apr 27, 2021 (155)
13 TOPMED ss5092213282 Apr 27, 2021 (155)
14 1000G_HIGH_COVERAGE ss5309170867 Oct 16, 2022 (156)
15 1000G_HIGH_COVERAGE ss5309170868 Oct 16, 2022 (156)
16 EVA ss5438081335 Oct 16, 2022 (156)
17 1000G_HIGH_COVERAGE ss5615803667 Oct 16, 2022 (156)
18 EVA ss5923851819 Oct 16, 2022 (156)
19 EVA ss5936428842 Oct 16, 2022 (156)
20 1000Genomes NC_000020.10 - 52786138 Oct 12, 2018 (152)
21 1000Genomes_30x NC_000020.11 - 54169599 Oct 16, 2022 (156)
22 ExAC

Submission ignored due to conflicting rows:
Row 5606856 (NC_000020.10:52786137:C:C 121372/121376, NC_000020.10:52786137:C:G 4/121376)
Row 5606857 (NC_000020.10:52786137:C:C 121341/121376, NC_000020.10:52786137:C:T 35/121376)

- Oct 12, 2018 (152)
23 ExAC

Submission ignored due to conflicting rows:
Row 5606856 (NC_000020.10:52786137:C:C 121372/121376, NC_000020.10:52786137:C:G 4/121376)
Row 5606857 (NC_000020.10:52786137:C:C 121341/121376, NC_000020.10:52786137:C:T 35/121376)

- Oct 12, 2018 (152)
24 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 554876604 (NC_000020.11:54169598:C:G 8/140274)
Row 554876605 (NC_000020.11:54169598:C:T 12/140274)

- Apr 27, 2021 (155)
25 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 554876604 (NC_000020.11:54169598:C:G 8/140274)
Row 554876605 (NC_000020.11:54169598:C:T 12/140274)

- Apr 27, 2021 (155)
26 gnomAD - Exomes

Submission ignored due to conflicting rows:
Row 14009830 (NC_000020.10:52786137:C:C 251418/251422, NC_000020.10:52786137:C:G 4/251422)
Row 14009831 (NC_000020.10:52786137:C:C 251322/251422, NC_000020.10:52786137:C:T 100/251422)

- Jul 13, 2019 (153)
27 gnomAD - Exomes

Submission ignored due to conflicting rows:
Row 14009830 (NC_000020.10:52786137:C:C 251418/251422, NC_000020.10:52786137:C:G 4/251422)
Row 14009831 (NC_000020.10:52786137:C:C 251322/251422, NC_000020.10:52786137:C:T 100/251422)

- Jul 13, 2019 (153)
28 GO Exome Sequencing Project NC_000020.10 - 52786138 Oct 12, 2018 (152)
29 TopMed

Submission ignored due to conflicting rows:
Row 367322226 (NC_000020.11:54169598:C:G 17/264690)
Row 367322227 (NC_000020.11:54169598:C:T 62/264690)

- Apr 27, 2021 (155)
30 TopMed

Submission ignored due to conflicting rows:
Row 367322226 (NC_000020.11:54169598:C:G 17/264690)
Row 367322227 (NC_000020.11:54169598:C:T 62/264690)

- Apr 27, 2021 (155)
31 ALFA NC_000020.11 - 54169599 Apr 27, 2021 (155)
32 ClinVar RCV000871491.3 Oct 16, 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).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
78666230, ss1365188341, ss1694048337, ss2744685947, ss2750406124, ss2968604548, ss5438081335, ss5936428842 NC_000020.10:52786137:C:G NC_000020.11:54169598:C:G (self)
103329602, 4718590571, ss5092213281, ss5309170867, ss5615803667, ss5923851819 NC_000020.11:54169598:C:G NC_000020.11:54169598:C:G (self)
ss1698891287 NC_000020.9:52219544:C:T NC_000020.11:54169598:C:T (self)
1839847, ss342525570, ss1694048338, ss2744685947, ss2750406124, ss2968604548, ss3825382950, ss5936428842 NC_000020.10:52786137:C:T NC_000020.11:54169598:C:T (self)
RCV000871491.3, 103329602, 4718590571, ss2243611363, ss3707158714, ss5092213282, ss5309170868, ss5615803667 NC_000020.11:54169598:C:T NC_000020.11:54169598:C:T (self)
Help

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

No publications for rs150102121

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.post774+babeb33