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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.

rs1476651136

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr19:53577920 (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>T
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.000004 (1/264690, TOPMED)
T=0.000014 (2/140276, GnomAD)
T=0.00000 (0/14050, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ZNF331 : Missense 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: 20231103111315
Population Group Sample Size Ref Allele Alt Allele Ref HMOZ Alt HMOZ HTRZ HWEP
Total Global 14050 C=1.00000 T=0.00000 1.0 0.0 0.0 N/A
European Sub 9690 C=1.0000 T=0.0000 1.0 0.0 0.0 N/A
African Sub 2898 C=1.0000 T=0.0000 1.0 0.0 0.0 N/A
African Others Sub 114 C=1.000 T=0.000 1.0 0.0 0.0 N/A
African American Sub 2784 C=1.0000 T=0.0000 1.0 0.0 0.0 N/A
Asian Sub 112 C=1.000 T=0.000 1.0 0.0 0.0 N/A
East Asian Sub 86 C=1.00 T=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 26 C=1.00 T=0.00 1.0 0.0 0.0 N/A
Latin American 1 Sub 146 C=1.000 T=0.000 1.0 0.0 0.0 N/A
Latin American 2 Sub 610 C=1.000 T=0.000 1.0 0.0 0.0 N/A
South Asian Sub 98 C=1.00 T=0.00 1.0 0.0 0.0 N/A
Other Sub 496 C=1.000 T=0.000 1.0 0.0 0.0 N/A


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 C=0.999996 T=0.000004
gnomAD - Genomes Global Study-wide 140276 C=0.999986 T=0.000014
gnomAD - Genomes European Sub 75960 C=1.00000 T=0.00000
gnomAD - Genomes African Sub 42060 C=0.99995 T=0.00005
gnomAD - Genomes American Sub 13654 C=1.00000 T=0.00000
gnomAD - Genomes Ashkenazi Jewish Sub 3322 C=1.0000 T=0.0000
gnomAD - Genomes East Asian Sub 3132 C=1.0000 T=0.0000
gnomAD - Genomes Other Sub 2148 C=1.0000 T=0.0000
Allele Frequency Aggregator Total Global 14050 C=1.00000 T=0.00000
Allele Frequency Aggregator European Sub 9690 C=1.0000 T=0.0000
Allele Frequency Aggregator African Sub 2898 C=1.0000 T=0.0000
Allele Frequency Aggregator Latin American 2 Sub 610 C=1.000 T=0.000
Allele Frequency Aggregator Other Sub 496 C=1.000 T=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 C=1.000 T=0.000
Allele Frequency Aggregator Asian Sub 112 C=1.000 T=0.000
Allele Frequency Aggregator South Asian Sub 98 C=1.00 T=0.00
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 19 NC_000019.10:g.53577920C>T
GRCh37.p13 chr 19 NC_000019.9:g.54081174C>T
ZNF331 RefSeqGene (LRG_1068) NG_045232.1:g.61998C>T
Gene: ZNF331, zinc finger protein 331 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
ZNF331 transcript variant 2 NM_001079907.1:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 NP_001073376.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant 7 NM_001253801.2:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 NP_001240730.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant 12 NM_001317117.1:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 NP_001304046.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant 13 NM_001317118.1:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 NP_001304047.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant 14 NM_001317119.1:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 NP_001304048.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant 16 NM_001317121.1:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 NP_001304050.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant 10 NM_001317115.2:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 NP_001304044.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant 3 NM_001253798.2:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 NP_001240727.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant 15 NM_001317120.2:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 NP_001304049.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant 5 NM_001253799.2:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 NP_001240728.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant 9 NM_001317114.2:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 NP_001304043.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant 1 NM_018555.6:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 NP_061025.5:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant 8 NM_001317113.2:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 NP_001304042.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant 4 NM_001079906.2:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 NP_001073375.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant 11 NM_001317116.2:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 NP_001304045.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant 6 NM_001253800.3:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 NP_001240729.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant X1 XM_047439049.1:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 isoform X1 XP_047295005.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant X2 XM_011527076.4:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 isoform X1 XP_011525378.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant X3 XM_047439050.1:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 isoform X1 XP_047295006.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant X4 XM_047439051.1:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 isoform X1 XP_047295007.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant X5 XM_011527078.4:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 isoform X1 XP_011525380.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant X6 XM_047439053.1:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 isoform X1 XP_047295009.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant X7 XM_047439054.1:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 isoform X1 XP_047295010.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant X8 XM_047439055.1:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 isoform X1 XP_047295011.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant X9 XM_047439056.1:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 isoform X1 XP_047295012.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant X10 XM_017026940.2:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 isoform X1 XP_016882429.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant X11 XM_047439057.1:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 isoform X1 XP_047295013.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant X12 XM_047439058.1:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 isoform X1 XP_047295014.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant X13 XM_047439059.1:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 isoform X1 XP_047295015.1:p.Leu454Phe L (Leu) > F (Phe) Missense Variant
ZNF331 transcript variant X14 XM_047439060.1:c.1360C>T L [CTC] > F [TTC] Coding Sequence Variant
zinc finger protein 331 isoform X1 XP_047295016.1:p.Leu454Phe L (Leu) > F (Phe) Missense 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
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= T
GRCh38.p14 chr 19 NC_000019.10:g.53577920= NC_000019.10:g.53577920C>T
GRCh37.p13 chr 19 NC_000019.9:g.54081174= NC_000019.9:g.54081174C>T
ZNF331 RefSeqGene (LRG_1068) NG_045232.1:g.61998= NG_045232.1:g.61998C>T
ZNF331 transcript variant 1 NM_018555.6:c.1360= NM_018555.6:c.1360C>T
ZNF331 transcript variant 1 NM_018555.5:c.1360= NM_018555.5:c.1360C>T
ZNF331 transcript variant 6 NM_001253800.3:c.1360= NM_001253800.3:c.1360C>T
ZNF331 transcript variant 6 NM_001253800.2:c.1360= NM_001253800.2:c.1360C>T
ZNF331 transcript variant 6 NM_001253800.1:c.1360= NM_001253800.1:c.1360C>T
ZNF331 transcript variant 15 NM_001317120.2:c.1360= NM_001317120.2:c.1360C>T
ZNF331 transcript variant 15 NM_001317120.1:c.1360= NM_001317120.1:c.1360C>T
ZNF331 transcript variant 9 NM_001317114.2:c.1360= NM_001317114.2:c.1360C>T
ZNF331 transcript variant 9 NM_001317114.1:c.1360= NM_001317114.1:c.1360C>T
ZNF331 transcript variant 3 NM_001253798.2:c.1360= NM_001253798.2:c.1360C>T
ZNF331 transcript variant 3 NM_001253798.1:c.1360= NM_001253798.1:c.1360C>T
ZNF331 transcript variant 5 NM_001253799.2:c.1360= NM_001253799.2:c.1360C>T
ZNF331 transcript variant 5 NM_001253799.1:c.1360= NM_001253799.1:c.1360C>T
ZNF331 transcript variant 10 NM_001317115.2:c.1360= NM_001317115.2:c.1360C>T
ZNF331 transcript variant 10 NM_001317115.1:c.1360= NM_001317115.1:c.1360C>T
ZNF331 transcript variant 4 NM_001079906.2:c.1360= NM_001079906.2:c.1360C>T
ZNF331 transcript variant 4 NM_001079906.1:c.1360= NM_001079906.1:c.1360C>T
ZNF331 transcript variant 7 NM_001253801.2:c.1360= NM_001253801.2:c.1360C>T
ZNF331 transcript variant 7 NM_001253801.1:c.1360= NM_001253801.1:c.1360C>T
ZNF331 transcript variant 8 NM_001317113.2:c.1360= NM_001317113.2:c.1360C>T
ZNF331 transcript variant 8 NM_001317113.1:c.1360= NM_001317113.1:c.1360C>T
ZNF331 transcript variant 11 NM_001317116.2:c.1360= NM_001317116.2:c.1360C>T
ZNF331 transcript variant 11 NM_001317116.1:c.1360= NM_001317116.1:c.1360C>T
ZNF331 transcript variant 13 NM_001317118.1:c.1360= NM_001317118.1:c.1360C>T
ZNF331 transcript variant 2 NM_001079907.1:c.1360= NM_001079907.1:c.1360C>T
ZNF331 transcript variant 14 NM_001317119.1:c.1360= NM_001317119.1:c.1360C>T
ZNF331 transcript variant 12 NM_001317117.1:c.1360= NM_001317117.1:c.1360C>T
ZNF331 transcript variant 16 NM_001317121.1:c.1360= NM_001317121.1:c.1360C>T
ZNF331 transcript variant X2 XM_011527076.4:c.1360= XM_011527076.4:c.1360C>T
ZNF331 transcript variant X8 XM_011527076.3:c.1360= XM_011527076.3:c.1360C>T
ZNF331 transcript variant X3 XM_011527076.2:c.1360= XM_011527076.2:c.1360C>T
ZNF331 transcript variant X3 XM_011527076.1:c.1360= XM_011527076.1:c.1360C>T
ZNF331 transcript variant X5 XM_011527078.4:c.1360= XM_011527078.4:c.1360C>T
ZNF331 transcript variant X11 XM_011527078.3:c.1360= XM_011527078.3:c.1360C>T
ZNF331 transcript variant X5 XM_011527078.2:c.1360= XM_011527078.2:c.1360C>T
ZNF331 transcript variant X6 XM_011527078.1:c.1360= XM_011527078.1:c.1360C>T
ZNF331 transcript variant X10 XM_017026940.2:c.1360= XM_017026940.2:c.1360C>T
ZNF331 transcript variant X13 XM_017026940.1:c.1360= XM_017026940.1:c.1360C>T
ZNF331 transcript variant X7 XM_047439054.1:c.1360= XM_047439054.1:c.1360C>T
ZNF331 transcript variant X3 XM_047439050.1:c.1360= XM_047439050.1:c.1360C>T
ZNF331 transcript variant X6 XM_047439053.1:c.1360= XM_047439053.1:c.1360C>T
ZNF331 transcript variant X4 XM_047439051.1:c.1360= XM_047439051.1:c.1360C>T
ZNF331 transcript variant X11 XM_047439057.1:c.1360= XM_047439057.1:c.1360C>T
ZNF331 transcript variant X8 XM_047439055.1:c.1360= XM_047439055.1:c.1360C>T
ZNF331 transcript variant X1 XM_047439049.1:c.1360= XM_047439049.1:c.1360C>T
ZNF331 transcript variant X13 XM_047439059.1:c.1360= XM_047439059.1:c.1360C>T
ZNF331 transcript variant X14 XM_047439060.1:c.1360= XM_047439060.1:c.1360C>T
ZNF331 transcript variant X12 XM_047439058.1:c.1360= XM_047439058.1:c.1360C>T
ZNF331 transcript variant X9 XM_047439056.1:c.1360= XM_047439056.1:c.1360C>T
zinc finger protein 331 NP_061025.5:p.Leu454= NP_061025.5:p.Leu454Phe
zinc finger protein 331 NP_001240729.1:p.Leu454= NP_001240729.1:p.Leu454Phe
zinc finger protein 331 NP_001304049.1:p.Leu454= NP_001304049.1:p.Leu454Phe
zinc finger protein 331 NP_001304043.1:p.Leu454= NP_001304043.1:p.Leu454Phe
zinc finger protein 331 NP_001240727.1:p.Leu454= NP_001240727.1:p.Leu454Phe
zinc finger protein 331 NP_001240728.1:p.Leu454= NP_001240728.1:p.Leu454Phe
zinc finger protein 331 NP_001304044.1:p.Leu454= NP_001304044.1:p.Leu454Phe
zinc finger protein 331 NP_001073375.1:p.Leu454= NP_001073375.1:p.Leu454Phe
zinc finger protein 331 NP_001240730.1:p.Leu454= NP_001240730.1:p.Leu454Phe
zinc finger protein 331 NP_001304042.1:p.Leu454= NP_001304042.1:p.Leu454Phe
zinc finger protein 331 NP_001304045.1:p.Leu454= NP_001304045.1:p.Leu454Phe
zinc finger protein 331 NP_001304047.1:p.Leu454= NP_001304047.1:p.Leu454Phe
zinc finger protein 331 NP_001073376.1:p.Leu454= NP_001073376.1:p.Leu454Phe
zinc finger protein 331 NP_001304048.1:p.Leu454= NP_001304048.1:p.Leu454Phe
zinc finger protein 331 NP_001304046.1:p.Leu454= NP_001304046.1:p.Leu454Phe
zinc finger protein 331 NP_001304050.1:p.Leu454= NP_001304050.1:p.Leu454Phe
zinc finger protein 331 isoform X1 XP_011525378.1:p.Leu454= XP_011525378.1:p.Leu454Phe
zinc finger protein 331 isoform X1 XP_011525380.1:p.Leu454= XP_011525380.1:p.Leu454Phe
zinc finger protein 331 isoform X1 XP_016882429.1:p.Leu454= XP_016882429.1:p.Leu454Phe
zinc finger protein 331 isoform X1 XP_047295010.1:p.Leu454= XP_047295010.1:p.Leu454Phe
zinc finger protein 331 isoform X1 XP_047295006.1:p.Leu454= XP_047295006.1:p.Leu454Phe
zinc finger protein 331 isoform X1 XP_047295009.1:p.Leu454= XP_047295009.1:p.Leu454Phe
zinc finger protein 331 isoform X1 XP_047295007.1:p.Leu454= XP_047295007.1:p.Leu454Phe
zinc finger protein 331 isoform X1 XP_047295013.1:p.Leu454= XP_047295013.1:p.Leu454Phe
zinc finger protein 331 isoform X1 XP_047295011.1:p.Leu454= XP_047295011.1:p.Leu454Phe
zinc finger protein 331 isoform X1 XP_047295005.1:p.Leu454= XP_047295005.1:p.Leu454Phe
zinc finger protein 331 isoform X1 XP_047295015.1:p.Leu454= XP_047295015.1:p.Leu454Phe
zinc finger protein 331 isoform X1 XP_047295016.1:p.Leu454= XP_047295016.1:p.Leu454Phe
zinc finger protein 331 isoform X1 XP_047295014.1:p.Leu454= XP_047295014.1:p.Leu454Phe
zinc finger protein 331 isoform X1 XP_047295012.1:p.Leu454= XP_047295012.1:p.Leu454Phe
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#.

2 SubSNP, 3 Frequency submissions
No Submitter Submission ID Date (Build)
1 GNOMAD ss4333091871 Apr 27, 2021 (155)
2 TOPMED ss5078379523 Apr 27, 2021 (155)
3 gnomAD - Genomes NC_000019.10 - 53577920 Apr 27, 2021 (155)
4 TopMed NC_000019.10 - 53577920 Apr 27, 2021 (155)
5 ALFA NC_000019.10 - 53577920 Apr 27, 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).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
543148702, 293925187, 1722016856, ss4333091871, ss5078379523 NC_000019.10:53577919:C:T NC_000019.10:53577919: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 rs1476651136

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.post820+afb47a3d