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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.

rs373409293

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr2:43824086 (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
A>G / A>T
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.000004 (1/264690, TOPMED)
G=0.000004 (1/251454, GnomAD_exome)
G=0.000008 (1/121340, ExAC) (+ 3 more)
T=0.00004 (1/28258, 14KJPN)
G=0.00007 (1/14050, ALFA)
G=0.00008 (1/13006, GO-ESP)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ABCG5 : Missense Variant
DYNC2LI1 : Intron 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 14050 A=0.99993 G=0.00007
European Sub 9690 A=1.0000 G=0.0000
African Sub 2898 A=0.9997 G=0.0003
African Others Sub 114 A=1.000 G=0.000
African American Sub 2784 A=0.9996 G=0.0004
Asian Sub 112 A=1.000 G=0.000
East Asian Sub 86 A=1.00 G=0.00
Other Asian Sub 26 A=1.00 G=0.00
Latin American 1 Sub 146 A=1.000 G=0.000
Latin American 2 Sub 610 A=1.000 G=0.000
South Asian Sub 98 A=1.00 G=0.00
Other Sub 496 A=1.000 G=0.000


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 A=0.999996 G=0.000004
gnomAD - Exomes Global Study-wide 251454 A=0.999996 G=0.000004
gnomAD - Exomes European Sub 135386 A=1.000000 G=0.000000
gnomAD - Exomes Asian Sub 49008 A=1.00000 G=0.00000
gnomAD - Exomes American Sub 34592 A=1.00000 G=0.00000
gnomAD - Exomes African Sub 16254 A=0.99994 G=0.00006
gnomAD - Exomes Ashkenazi Jewish Sub 10078 A=1.00000 G=0.00000
gnomAD - Exomes Other Sub 6136 A=1.0000 G=0.0000
ExAC Global Study-wide 121340 A=0.999992 G=0.000008
ExAC Europe Sub 73346 A=1.00000 G=0.00000
ExAC Asian Sub 25158 A=1.00000 G=0.00000
ExAC American Sub 11576 A=1.00000 G=0.00000
ExAC African Sub 10352 A=0.99990 G=0.00010
ExAC Other Sub 908 A=1.000 G=0.000
14KJPN JAPANESE Study-wide 28258 A=0.99996 T=0.00004
Allele Frequency Aggregator Total Global 14050 A=0.99993 G=0.00007
Allele Frequency Aggregator European Sub 9690 A=1.0000 G=0.0000
Allele Frequency Aggregator African Sub 2898 A=0.9997 G=0.0003
Allele Frequency Aggregator Latin American 2 Sub 610 A=1.000 G=0.000
Allele Frequency Aggregator Other Sub 496 A=1.000 G=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 A=1.000 G=0.000
Allele Frequency Aggregator Asian Sub 112 A=1.000 G=0.000
Allele Frequency Aggregator South Asian Sub 98 A=1.00 G=0.00
GO Exome Sequencing Project Global Study-wide 13006 A=0.99992 G=0.00008
GO Exome Sequencing Project European American Sub 8600 A=1.0000 G=0.0000
GO Exome Sequencing Project African American Sub 4406 A=0.9998 G=0.0002
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 2 NC_000002.12:g.43824086A>G
GRCh38.p14 chr 2 NC_000002.12:g.43824086A>T
GRCh37.p13 chr 2 NC_000002.11:g.44051225A>G
GRCh37.p13 chr 2 NC_000002.11:g.44051225A>T
DYNC2LI1 RefSeqGene NG_053008.1:g.55048A>G
DYNC2LI1 RefSeqGene NG_053008.1:g.55048A>T
ABCG5 RefSeqGene (LRG_1181) NG_008883.1:g.19734T>C
ABCG5 RefSeqGene (LRG_1181) NG_008883.1:g.19734T>A
Gene: DYNC2LI1, dynein cytoplasmic 2 light intermediate chain 1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
DYNC2LI1 transcript variant 5 NM_001348912.2:c.*16-3300…

NM_001348912.2:c.*16-3300A>G

N/A Intron Variant
DYNC2LI1 transcript variant 6 NM_001348913.2:c.*16-3300…

NM_001348913.2:c.*16-3300A>G

N/A Intron Variant
DYNC2LI1 transcript variant 4 NM_001193464.2:c. N/A Genic Downstream Transcript Variant
DYNC2LI1 transcript variant 2 NM_015522.4:c. N/A Genic Downstream Transcript Variant
DYNC2LI1 transcript variant 1 NM_016008.4:c. N/A Genic Downstream Transcript Variant
Gene: ABCG5, ATP binding cassette subfamily G member 5 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
ABCG5 transcript NM_022436.3:c.1151T>C L [CTG] > P [CCG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 NP_071881.1:p.Leu384Pro L (Leu) > P (Pro) Missense Variant
ABCG5 transcript NM_022436.3:c.1151T>A L [CTG] > Q [CAG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 NP_071881.1:p.Leu384Gln L (Leu) > Q (Gln) Missense Variant
ABCG5 transcript variant X11 XM_006712074.4:c. N/A Genic Downstream Transcript Variant
ABCG5 transcript variant X1 XM_011533024.3:c.1151T>C L [CTG] > P [CCG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 isoform X1 XP_011531326.1:p.Leu384Pro L (Leu) > P (Pro) Missense Variant
ABCG5 transcript variant X1 XM_011533024.3:c.1151T>A L [CTG] > Q [CAG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 isoform X1 XP_011531326.1:p.Leu384Gln L (Leu) > Q (Gln) Missense Variant
ABCG5 transcript variant X2 XM_006712073.4:c.1151T>C L [CTG] > P [CCG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 isoform X2 XP_006712136.1:p.Leu384Pro L (Leu) > P (Pro) Missense Variant
ABCG5 transcript variant X2 XM_006712073.4:c.1151T>A L [CTG] > Q [CAG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 isoform X2 XP_006712136.1:p.Leu384Gln L (Leu) > Q (Gln) Missense Variant
ABCG5 transcript variant X3 XM_011533025.4:c.908T>C L [CTG] > P [CCG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 isoform X3 XP_011531327.1:p.Leu303Pro L (Leu) > P (Pro) Missense Variant
ABCG5 transcript variant X3 XM_011533025.4:c.908T>A L [CTG] > Q [CAG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 isoform X3 XP_011531327.1:p.Leu303Gln L (Leu) > Q (Gln) Missense Variant
ABCG5 transcript variant X4 XM_047445409.1:c.908T>C L [CTG] > P [CCG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 isoform X3 XP_047301365.1:p.Leu303Pro L (Leu) > P (Pro) Missense Variant
ABCG5 transcript variant X4 XM_047445409.1:c.908T>A L [CTG] > Q [CAG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 isoform X3 XP_047301365.1:p.Leu303Gln L (Leu) > Q (Gln) Missense Variant
ABCG5 transcript variant X5 XM_011533026.3:c.881T>C L [CTG] > P [CCG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 isoform X4 XP_011531328.1:p.Leu294Pro L (Leu) > P (Pro) Missense Variant
ABCG5 transcript variant X5 XM_011533026.3:c.881T>A L [CTG] > Q [CAG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 isoform X4 XP_011531328.1:p.Leu294Gln L (Leu) > Q (Gln) Missense Variant
ABCG5 transcript variant X6 XM_005264480.5:c.1151T>C L [CTG] > P [CCG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 isoform X5 XP_005264537.1:p.Leu384Pro L (Leu) > P (Pro) Missense Variant
ABCG5 transcript variant X6 XM_005264480.5:c.1151T>A L [CTG] > Q [CAG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 isoform X5 XP_005264537.1:p.Leu384Gln L (Leu) > Q (Gln) Missense Variant
ABCG5 transcript variant X7 XM_011533027.4:c.638T>C L [CTG] > P [CCG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 isoform X6 XP_011531329.1:p.Leu213Pro L (Leu) > P (Pro) Missense Variant
ABCG5 transcript variant X7 XM_011533027.4:c.638T>A L [CTG] > Q [CAG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 isoform X6 XP_011531329.1:p.Leu213Gln L (Leu) > Q (Gln) Missense Variant
ABCG5 transcript variant X8 XM_047445410.1:c.638T>C L [CTG] > P [CCG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 isoform X7 XP_047301366.1:p.Leu213Pro L (Leu) > P (Pro) Missense Variant
ABCG5 transcript variant X8 XM_047445410.1:c.638T>A L [CTG] > Q [CAG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 isoform X7 XP_047301366.1:p.Leu213Gln L (Leu) > Q (Gln) Missense Variant
ABCG5 transcript variant X9 XM_047445411.1:c.638T>C L [CTG] > P [CCG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 isoform X8 XP_047301367.1:p.Leu213Pro L (Leu) > P (Pro) Missense Variant
ABCG5 transcript variant X9 XM_047445411.1:c.638T>A L [CTG] > Q [CAG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 isoform X8 XP_047301367.1:p.Leu213Gln L (Leu) > Q (Gln) Missense Variant
ABCG5 transcript variant X10 XM_011533028.3:c.314T>C L [CTG] > P [CCG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 isoform X9 XP_011531330.1:p.Leu105Pro L (Leu) > P (Pro) Missense Variant
ABCG5 transcript variant X10 XM_011533028.3:c.314T>A L [CTG] > Q [CAG] Coding Sequence Variant
ATP-binding cassette sub-family G member 5 isoform X9 XP_011531330.1:p.Leu105Gln L (Leu) > Q (Gln) 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 A= G T
GRCh38.p14 chr 2 NC_000002.12:g.43824086= NC_000002.12:g.43824086A>G NC_000002.12:g.43824086A>T
GRCh37.p13 chr 2 NC_000002.11:g.44051225= NC_000002.11:g.44051225A>G NC_000002.11:g.44051225A>T
DYNC2LI1 RefSeqGene NG_053008.1:g.55048= NG_053008.1:g.55048A>G NG_053008.1:g.55048A>T
ABCG5 RefSeqGene (LRG_1181) NG_008883.1:g.19734= NG_008883.1:g.19734T>C NG_008883.1:g.19734T>A
ABCG5 transcript NM_022436.3:c.1151= NM_022436.3:c.1151T>C NM_022436.3:c.1151T>A
ABCG5 transcript NM_022436.2:c.1151= NM_022436.2:c.1151T>C NM_022436.2:c.1151T>A
ABCG5 transcript variant X6 XM_005264480.5:c.1151= XM_005264480.5:c.1151T>C XM_005264480.5:c.1151T>A
ABCG5 transcript variant X5 XM_005264480.4:c.1151= XM_005264480.4:c.1151T>C XM_005264480.4:c.1151T>A
ABCG5 transcript variant X5 XM_005264480.3:c.1151= XM_005264480.3:c.1151T>C XM_005264480.3:c.1151T>A
ABCG5 transcript variant X5 XM_005264480.2:c.1151= XM_005264480.2:c.1151T>C XM_005264480.2:c.1151T>A
ABCG5 transcript variant X1 XM_005264480.1:c.1151= XM_005264480.1:c.1151T>C XM_005264480.1:c.1151T>A
ABCG5 transcript variant X3 XM_011533025.4:c.908= XM_011533025.4:c.908T>C XM_011533025.4:c.908T>A
ABCG5 transcript variant X3 XM_011533025.3:c.908= XM_011533025.3:c.908T>C XM_011533025.3:c.908T>A
ABCG5 transcript variant X3 XM_011533025.2:c.908= XM_011533025.2:c.908T>C XM_011533025.2:c.908T>A
ABCG5 transcript variant X3 XM_011533025.1:c.908= XM_011533025.1:c.908T>C XM_011533025.1:c.908T>A
ABCG5 transcript variant X7 XM_011533027.4:c.638= XM_011533027.4:c.638T>C XM_011533027.4:c.638T>A
ABCG5 transcript variant X6 XM_011533027.3:c.638= XM_011533027.3:c.638T>C XM_011533027.3:c.638T>A
ABCG5 transcript variant X6 XM_011533027.2:c.638= XM_011533027.2:c.638T>C XM_011533027.2:c.638T>A
ABCG5 transcript variant X6 XM_011533027.1:c.638= XM_011533027.1:c.638T>C XM_011533027.1:c.638T>A
ABCG5 transcript variant X2 XM_006712073.4:c.1151= XM_006712073.4:c.1151T>C XM_006712073.4:c.1151T>A
ABCG5 transcript variant X2 XM_006712073.3:c.1151= XM_006712073.3:c.1151T>C XM_006712073.3:c.1151T>A
ABCG5 transcript variant X2 XM_006712073.2:c.1151= XM_006712073.2:c.1151T>C XM_006712073.2:c.1151T>A
ABCG5 transcript variant X3 XM_006712073.1:c.1151= XM_006712073.1:c.1151T>C XM_006712073.1:c.1151T>A
ABCG5 transcript variant X1 XM_011533024.3:c.1151= XM_011533024.3:c.1151T>C XM_011533024.3:c.1151T>A
ABCG5 transcript variant X1 XM_011533024.2:c.1151= XM_011533024.2:c.1151T>C XM_011533024.2:c.1151T>A
ABCG5 transcript variant X1 XM_011533024.1:c.1151= XM_011533024.1:c.1151T>C XM_011533024.1:c.1151T>A
ABCG5 transcript variant X5 XM_011533026.3:c.881= XM_011533026.3:c.881T>C XM_011533026.3:c.881T>A
ABCG5 transcript variant X4 XM_011533026.2:c.881= XM_011533026.2:c.881T>C XM_011533026.2:c.881T>A
ABCG5 transcript variant X4 XM_011533026.1:c.881= XM_011533026.1:c.881T>C XM_011533026.1:c.881T>A
ABCG5 transcript variant X10 XM_011533028.3:c.314= XM_011533028.3:c.314T>C XM_011533028.3:c.314T>A
ABCG5 transcript variant X7 XM_011533028.2:c.314= XM_011533028.2:c.314T>C XM_011533028.2:c.314T>A
ABCG5 transcript variant X7 XM_011533028.1:c.314= XM_011533028.1:c.314T>C XM_011533028.1:c.314T>A
ABCG5 transcript variant X9 XM_047445411.1:c.638= XM_047445411.1:c.638T>C XM_047445411.1:c.638T>A
ABCG5 transcript variant X4 XM_047445409.1:c.908= XM_047445409.1:c.908T>C XM_047445409.1:c.908T>A
ABCG5 transcript variant X8 XM_047445410.1:c.638= XM_047445410.1:c.638T>C XM_047445410.1:c.638T>A
ATP-binding cassette sub-family G member 5 NP_071881.1:p.Leu384= NP_071881.1:p.Leu384Pro NP_071881.1:p.Leu384Gln
ATP-binding cassette sub-family G member 5 isoform X5 XP_005264537.1:p.Leu384= XP_005264537.1:p.Leu384Pro XP_005264537.1:p.Leu384Gln
ATP-binding cassette sub-family G member 5 isoform X3 XP_011531327.1:p.Leu303= XP_011531327.1:p.Leu303Pro XP_011531327.1:p.Leu303Gln
ATP-binding cassette sub-family G member 5 isoform X6 XP_011531329.1:p.Leu213= XP_011531329.1:p.Leu213Pro XP_011531329.1:p.Leu213Gln
ATP-binding cassette sub-family G member 5 isoform X2 XP_006712136.1:p.Leu384= XP_006712136.1:p.Leu384Pro XP_006712136.1:p.Leu384Gln
ATP-binding cassette sub-family G member 5 isoform X1 XP_011531326.1:p.Leu384= XP_011531326.1:p.Leu384Pro XP_011531326.1:p.Leu384Gln
ATP-binding cassette sub-family G member 5 isoform X4 XP_011531328.1:p.Leu294= XP_011531328.1:p.Leu294Pro XP_011531328.1:p.Leu294Gln
ATP-binding cassette sub-family G member 5 isoform X9 XP_011531330.1:p.Leu105= XP_011531330.1:p.Leu105Pro XP_011531330.1:p.Leu105Gln
ATP-binding cassette sub-family G member 5 isoform X8 XP_047301367.1:p.Leu213= XP_047301367.1:p.Leu213Pro XP_047301367.1:p.Leu213Gln
ATP-binding cassette sub-family G member 5 isoform X3 XP_047301365.1:p.Leu303= XP_047301365.1:p.Leu303Pro XP_047301365.1:p.Leu303Gln
ATP-binding cassette sub-family G member 5 isoform X7 XP_047301366.1:p.Leu213= XP_047301366.1:p.Leu213Pro XP_047301366.1:p.Leu213Gln
DYNC2LI1 transcript variant 5 NM_001348912.2:c.*16-3300= NM_001348912.2:c.*16-3300A>G NM_001348912.2:c.*16-3300A>T
DYNC2LI1 transcript variant 6 NM_001348913.2:c.*16-3300= NM_001348913.2:c.*16-3300A>G NM_001348913.2:c.*16-3300A>T
DYNC2LI1 transcript variant X1 XM_005264364.1:c.*16-3300= XM_005264364.1:c.*16-3300A>G XM_005264364.1:c.*16-3300A>T
DYNC2LI1 transcript variant X2 XM_005264365.1:c.*16-3300= XM_005264365.1:c.*16-3300A>G XM_005264365.1:c.*16-3300A>T
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#.

6 SubSNP, 6 Frequency submissions
No Submitter Submission ID Date (Build)
1 NHLBI-ESP ss712413611 Apr 25, 2013 (138)
2 EVA_EXAC ss1686287247 Apr 01, 2015 (144)
3 GNOMAD ss2732633692 Nov 08, 2017 (151)
4 EVA ss3823765193 Apr 25, 2020 (154)
5 TOPMED ss4502977961 Apr 26, 2021 (155)
6 TOMMO_GENOMICS ss5679541570 Oct 12, 2022 (156)
7 ExAC NC_000002.11 - 44051225 Oct 11, 2018 (152)
8 gnomAD - Exomes NC_000002.11 - 44051225 Jul 13, 2019 (153)
9 GO Exome Sequencing Project NC_000002.11 - 44051225 Oct 11, 2018 (152)
10 14KJPN NC_000002.12 - 43824086 Oct 12, 2022 (156)
11 TopMed NC_000002.12 - 43824086 Apr 26, 2021 (155)
12 ALFA NC_000002.12 - 43824086 Apr 26, 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
6155886, 1680560, 223663, ss712413611, ss1686287247, ss2732633692, ss3823765193 NC_000002.11:44051224:A:G NC_000002.12:43824085:A:G (self)
306800840, 3931199129, ss4502977961 NC_000002.12:43824085:A:G NC_000002.12:43824085:A:G (self)
13378674, ss5679541570 NC_000002.12:43824085:A:T NC_000002.12:43824085:A:T
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 rs373409293

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