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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.

rs762619940

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr10:27860747 (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=0.000007 (1/140224, GnomAD)
A=0.000008 (1/121340, ExAC)
A=0.00005 (1/21350, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ODAD2 : 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: 20230706150541
Population Group Sample Size Ref Allele Alt Allele
Total Global 21350 G=0.99995 A=0.00005
European Sub 16878 G=0.99994 A=0.00006
African Sub 20 G=1.00 A=0.00
African Others Sub 0 G=0 A=0
African American Sub 20 G=1.00 A=0.00
Asian Sub 0 G=0 A=0
East Asian Sub 0 G=0 A=0
Other Asian Sub 0 G=0 A=0
Latin American 1 Sub 354 G=1.000 A=0.000
Latin American 2 Sub 18 G=1.00 A=0.00
South Asian Sub 0 G=0 A=0
Other Sub 4080 G=1.0000 A=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
gnomAD - Genomes Global Study-wide 140224 G=0.999993 A=0.000007
gnomAD - Genomes European Sub 75952 G=0.99999 A=0.00001
gnomAD - Genomes African Sub 42022 G=1.00000 A=0.00000
gnomAD - Genomes American Sub 13654 G=1.00000 A=0.00000
gnomAD - Genomes Ashkenazi Jewish Sub 3318 G=1.0000 A=0.0000
gnomAD - Genomes East Asian Sub 3126 G=1.0000 A=0.0000
gnomAD - Genomes Other Sub 2152 G=1.0000 A=0.0000
ExAC Global Study-wide 121340 G=0.999992 A=0.000008
ExAC Europe Sub 73336 G=0.99999 A=0.00001
ExAC Asian Sub 25154 G=1.00000 A=0.00000
ExAC American Sub 11540 G=1.00000 A=0.00000
ExAC African Sub 10402 G=1.00000 A=0.00000
ExAC Other Sub 908 G=1.000 A=0.000
Allele Frequency Aggregator Total Global 21350 G=0.99995 A=0.00005
Allele Frequency Aggregator European Sub 16878 G=0.99994 A=0.00006
Allele Frequency Aggregator Other Sub 4080 G=1.0000 A=0.0000
Allele Frequency Aggregator Latin American 1 Sub 354 G=1.000 A=0.000
Allele Frequency Aggregator African Sub 20 G=1.00 A=0.00
Allele Frequency Aggregator Latin American 2 Sub 18 G=1.00 A=0.00
Allele Frequency Aggregator South Asian Sub 0 G=0 A=0
Allele Frequency Aggregator Asian Sub 0 G=0 A=0
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 10 NC_000010.11:g.27860747G>A
GRCh37.p13 chr 10 NC_000010.10:g.28149676G>A
ODAD2 RefSeqGene NG_042820.1:g.143304C>T
Gene: ODAD2, outer dynein arm docking complex subunit 2 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
ODAD2 transcript variant 3 NM_018076.5:c.2899C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform 1 NP_060546.2:p.Pro967Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant 2 NM_001290021.2:c.1474C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform 2 NP_001276950.1:p.Pro492Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant 4 NM_001312689.2:c.1975C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform 3 NP_001299618.1:p.Pro659Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant 1 NM_001290020.2:c.2899C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform 1 NP_001276949.1:p.Pro967Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X23 XM_017016371.2:c. N/A Genic Downstream Transcript Variant
ODAD2 transcript variant X1 XM_024448051.2:c.3028C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X1 XP_024303819.1:p.Pro1010S…

XP_024303819.1:p.Pro1010Ser

P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X2 XM_024448049.2:c.3028C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X1 XP_024303817.1:p.Pro1010S…

XP_024303817.1:p.Pro1010Ser

P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X3 XM_024448050.2:c.3028C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X1 XP_024303818.1:p.Pro1010S…

XP_024303818.1:p.Pro1010Ser

P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X4 XM_024448052.2:c.3028C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X1 XP_024303820.1:p.Pro1010S…

XP_024303820.1:p.Pro1010Ser

P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X5 XM_024448053.2:c.3028C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X2 XP_024303821.1:p.Pro1010S…

XP_024303821.1:p.Pro1010Ser

P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X6 XM_011519527.2:c.2899C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X3 XP_011517829.1:p.Pro967Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X7 XM_047425401.1:c.2899C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X3 XP_047281357.1:p.Pro967Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X8 XM_047425402.1:c.2899C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X4 XP_047281358.1:p.Pro967Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X9 XM_047425403.1:c.2899C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X4 XP_047281359.1:p.Pro967Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X10 XM_047425404.1:c.2899C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X4 XP_047281360.1:p.Pro967Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X11 XM_047425405.1:c.2818C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X5 XP_047281361.1:p.Pro940Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X12 XM_047425407.1:c.2689C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X6 XP_047281363.1:p.Pro897Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X13 XM_047425408.1:c.2689C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X6 XP_047281364.1:p.Pro897Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X14 XM_047425409.1:c.2689C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X7 XP_047281365.1:p.Pro897Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X15 XM_047425410.1:c.2689C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X7 XP_047281366.1:p.Pro897Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X16 XM_047425411.1:c.2527C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X8 XP_047281367.1:p.Pro843Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X17 XM_047425412.1:c.2527C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X8 XP_047281368.1:p.Pro843Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X18 XM_047425413.1:c.2527C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X8 XP_047281369.1:p.Pro843Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X19 XM_047425414.1:c.2317C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X9 XP_047281370.1:p.Pro773Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X20 XM_024448055.2:c.2104C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X10 XP_024303823.1:p.Pro702Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X21 XM_024448056.2:c.2104C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X10 XP_024303824.1:p.Pro702Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X22 XM_024448057.2:c.1942C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X11 XP_024303825.1:p.Pro648Ser P (Pro) > S (Ser) Missense Variant
ODAD2 transcript variant X24 XM_024448058.2:c.1603C>T P [CCA] > S [TCA] Coding Sequence Variant
outer dynein arm-docking complex subunit 2 isoform X13 XP_024303826.1:p.Pro535Ser P (Pro) > S (Ser) 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 G= A
GRCh38.p14 chr 10 NC_000010.11:g.27860747= NC_000010.11:g.27860747G>A
GRCh37.p13 chr 10 NC_000010.10:g.28149676= NC_000010.10:g.28149676G>A
ODAD2 RefSeqGene NG_042820.1:g.143304= NG_042820.1:g.143304C>T
ODAD2 transcript variant 3 NM_018076.5:c.2899= NM_018076.5:c.2899C>T
ARMC4 transcript variant 3 NM_018076.4:c.2899= NM_018076.4:c.2899C>T
ARMC4 transcript variant 3 NM_018076.3:c.2899= NM_018076.3:c.2899C>T
ARMC4 transcript NM_018076.2:c.2899= NM_018076.2:c.2899C>T
ODAD2 transcript variant 1 NM_001290020.2:c.2899= NM_001290020.2:c.2899C>T
ARMC4 transcript variant 1 NM_001290020.1:c.2899= NM_001290020.1:c.2899C>T
ODAD2 transcript variant 4 NM_001312689.2:c.1975= NM_001312689.2:c.1975C>T
ARMC4 transcript variant 4 NM_001312689.1:c.1975= NM_001312689.1:c.1975C>T
ODAD2 transcript variant 2 NM_001290021.2:c.1474= NM_001290021.2:c.1474C>T
ARMC4 transcript variant 2 NM_001290021.1:c.1474= NM_001290021.1:c.1474C>T
ODAD2 transcript variant X3 XM_024448050.2:c.3028= XM_024448050.2:c.3028C>T
ODAD2 transcript variant X2 XM_024448050.1:c.3028= XM_024448050.1:c.3028C>T
ODAD2 transcript variant X4 XM_024448052.2:c.3028= XM_024448052.2:c.3028C>T
ODAD2 transcript variant X4 XM_024448052.1:c.3028= XM_024448052.1:c.3028C>T
ODAD2 transcript variant X2 XM_024448049.2:c.3028= XM_024448049.2:c.3028C>T
ODAD2 transcript variant X1 XM_024448049.1:c.3028= XM_024448049.1:c.3028C>T
ODAD2 transcript variant X1 XM_024448051.2:c.3028= XM_024448051.2:c.3028C>T
ODAD2 transcript variant X3 XM_024448051.1:c.3028= XM_024448051.1:c.3028C>T
ODAD2 transcript variant X5 XM_024448053.2:c.3028= XM_024448053.2:c.3028C>T
ODAD2 transcript variant X5 XM_024448053.1:c.3028= XM_024448053.1:c.3028C>T
ODAD2 transcript variant X6 XM_011519527.2:c.2899= XM_011519527.2:c.2899C>T
ODAD2 transcript variant X6 XM_011519527.1:c.2899= XM_011519527.1:c.2899C>T
ODAD2 transcript variant X20 XM_024448055.2:c.2104= XM_024448055.2:c.2104C>T
ODAD2 transcript variant X8 XM_024448055.1:c.2104= XM_024448055.1:c.2104C>T
ODAD2 transcript variant X21 XM_024448056.2:c.2104= XM_024448056.2:c.2104C>T
ODAD2 transcript variant X9 XM_024448056.1:c.2104= XM_024448056.1:c.2104C>T
ODAD2 transcript variant X22 XM_024448057.2:c.1942= XM_024448057.2:c.1942C>T
ODAD2 transcript variant X10 XM_024448057.1:c.1942= XM_024448057.1:c.1942C>T
ODAD2 transcript variant X24 XM_024448058.2:c.1603= XM_024448058.2:c.1603C>T
ODAD2 transcript variant X12 XM_024448058.1:c.1603= XM_024448058.1:c.1603C>T
ODAD2 transcript variant X8 XM_047425402.1:c.2899= XM_047425402.1:c.2899C>T
ODAD2 transcript variant X9 XM_047425403.1:c.2899= XM_047425403.1:c.2899C>T
ODAD2 transcript variant X17 XM_047425412.1:c.2527= XM_047425412.1:c.2527C>T
ODAD2 transcript variant X10 XM_047425404.1:c.2899= XM_047425404.1:c.2899C>T
ODAD2 transcript variant X7 XM_047425401.1:c.2899= XM_047425401.1:c.2899C>T
ODAD2 transcript variant X11 XM_047425405.1:c.2818= XM_047425405.1:c.2818C>T
ODAD2 transcript variant X12 XM_047425407.1:c.2689= XM_047425407.1:c.2689C>T
ODAD2 transcript variant X16 XM_047425411.1:c.2527= XM_047425411.1:c.2527C>T
ODAD2 transcript variant X13 XM_047425408.1:c.2689= XM_047425408.1:c.2689C>T
ODAD2 transcript variant X18 XM_047425413.1:c.2527= XM_047425413.1:c.2527C>T
ODAD2 transcript variant X14 XM_047425409.1:c.2689= XM_047425409.1:c.2689C>T
ODAD2 transcript variant X15 XM_047425410.1:c.2689= XM_047425410.1:c.2689C>T
ODAD2 transcript variant X19 XM_047425414.1:c.2317= XM_047425414.1:c.2317C>T
DKFZP434P1735 transcript NM_032150.1:c.1282= NM_032150.1:c.1282C>T
outer dynein arm-docking complex subunit 2 isoform 1 NP_060546.2:p.Pro967= NP_060546.2:p.Pro967Ser
outer dynein arm-docking complex subunit 2 isoform 1 NP_001276949.1:p.Pro967= NP_001276949.1:p.Pro967Ser
outer dynein arm-docking complex subunit 2 isoform 3 NP_001299618.1:p.Pro659= NP_001299618.1:p.Pro659Ser
outer dynein arm-docking complex subunit 2 isoform 2 NP_001276950.1:p.Pro492= NP_001276950.1:p.Pro492Ser
outer dynein arm-docking complex subunit 2 isoform X1 XP_024303818.1:p.Pro1010= XP_024303818.1:p.Pro1010Ser
outer dynein arm-docking complex subunit 2 isoform X1 XP_024303820.1:p.Pro1010= XP_024303820.1:p.Pro1010Ser
outer dynein arm-docking complex subunit 2 isoform X1 XP_024303817.1:p.Pro1010= XP_024303817.1:p.Pro1010Ser
outer dynein arm-docking complex subunit 2 isoform X1 XP_024303819.1:p.Pro1010= XP_024303819.1:p.Pro1010Ser
outer dynein arm-docking complex subunit 2 isoform X2 XP_024303821.1:p.Pro1010= XP_024303821.1:p.Pro1010Ser
outer dynein arm-docking complex subunit 2 isoform X3 XP_011517829.1:p.Pro967= XP_011517829.1:p.Pro967Ser
outer dynein arm-docking complex subunit 2 isoform X10 XP_024303823.1:p.Pro702= XP_024303823.1:p.Pro702Ser
outer dynein arm-docking complex subunit 2 isoform X10 XP_024303824.1:p.Pro702= XP_024303824.1:p.Pro702Ser
outer dynein arm-docking complex subunit 2 isoform X11 XP_024303825.1:p.Pro648= XP_024303825.1:p.Pro648Ser
outer dynein arm-docking complex subunit 2 isoform X13 XP_024303826.1:p.Pro535= XP_024303826.1:p.Pro535Ser
outer dynein arm-docking complex subunit 2 isoform X4 XP_047281358.1:p.Pro967= XP_047281358.1:p.Pro967Ser
outer dynein arm-docking complex subunit 2 isoform X4 XP_047281359.1:p.Pro967= XP_047281359.1:p.Pro967Ser
outer dynein arm-docking complex subunit 2 isoform X8 XP_047281368.1:p.Pro843= XP_047281368.1:p.Pro843Ser
outer dynein arm-docking complex subunit 2 isoform X4 XP_047281360.1:p.Pro967= XP_047281360.1:p.Pro967Ser
outer dynein arm-docking complex subunit 2 isoform X3 XP_047281357.1:p.Pro967= XP_047281357.1:p.Pro967Ser
outer dynein arm-docking complex subunit 2 isoform X5 XP_047281361.1:p.Pro940= XP_047281361.1:p.Pro940Ser
outer dynein arm-docking complex subunit 2 isoform X6 XP_047281363.1:p.Pro897= XP_047281363.1:p.Pro897Ser
outer dynein arm-docking complex subunit 2 isoform X8 XP_047281367.1:p.Pro843= XP_047281367.1:p.Pro843Ser
outer dynein arm-docking complex subunit 2 isoform X6 XP_047281364.1:p.Pro897= XP_047281364.1:p.Pro897Ser
outer dynein arm-docking complex subunit 2 isoform X8 XP_047281369.1:p.Pro843= XP_047281369.1:p.Pro843Ser
outer dynein arm-docking complex subunit 2 isoform X7 XP_047281365.1:p.Pro897= XP_047281365.1:p.Pro897Ser
outer dynein arm-docking complex subunit 2 isoform X7 XP_047281366.1:p.Pro897= XP_047281366.1:p.Pro897Ser
outer dynein arm-docking complex subunit 2 isoform X9 XP_047281370.1:p.Pro773= XP_047281370.1:p.Pro773Ser
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 EVA_EXAC ss1689857428 Apr 01, 2015 (144)
2 GNOMAD ss4215181398 Apr 26, 2021 (155)
3 ExAC NC_000010.10 - 28149676 Oct 12, 2018 (152)
4 gnomAD - Genomes NC_000010.11 - 27860747 Apr 26, 2021 (155)
5 ALFA NC_000010.11 - 27860747 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
75088, ss1689857428 NC_000010.10:28149675:G:A NC_000010.11:27860746:G:A (self)
347193449, 13778660324, ss4215181398 NC_000010.11:27860746:G:A NC_000010.11:27860746: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.

No publications for rs762619940

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