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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.

rs75124279

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr10:48438328 (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
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.008931 (2364/264690, TOPMED)
G=0.008656 (1214/140252, GnomAD)
G=0.00589 (85/14420, ALFA) (+ 8 more)
G=0.0089 (57/6404, 1000G_30x)
G=0.0086 (43/5008, 1000G)
G=0.0003 (1/3854, ALSPAC)
G=0.0000 (0/3708, TWINSUK)
G=0.001 (1/998, GoNL)
G=0.009 (2/216, Qatari)
A=0.5 (3/6, SGDP_PRJ)
G=0.5 (3/6, SGDP_PRJ)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
MAPK8 : Non Coding Transcript Variant
ARHGAP22 : 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 14420 A=0.99411 G=0.00589
European Sub 9824 A=1.0000 G=0.0000
African Sub 2946 A=0.9732 G=0.0268
African Others Sub 114 A=0.974 G=0.026
African American Sub 2832 A=0.9732 G=0.0268
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=0.986 G=0.014
Latin American 2 Sub 610 A=0.998 G=0.002
South Asian Sub 98 A=1.00 G=0.00
Other Sub 684 A=0.996 G=0.004


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=0.991069 G=0.008931
gnomAD - Genomes Global Study-wide 140252 A=0.991344 G=0.008656
gnomAD - Genomes European Sub 75946 A=0.99989 G=0.00011
gnomAD - Genomes African Sub 42042 A=0.97293 G=0.02707
gnomAD - Genomes American Sub 13662 A=0.99605 G=0.00395
gnomAD - Genomes Ashkenazi Jewish Sub 3322 A=1.0000 G=0.0000
gnomAD - Genomes East Asian Sub 3128 A=1.0000 G=0.0000
gnomAD - Genomes Other Sub 2152 A=0.9935 G=0.0065
Allele Frequency Aggregator Total Global 14420 A=0.99411 G=0.00589
Allele Frequency Aggregator European Sub 9824 A=1.0000 G=0.0000
Allele Frequency Aggregator African Sub 2946 A=0.9732 G=0.0268
Allele Frequency Aggregator Other Sub 684 A=0.996 G=0.004
Allele Frequency Aggregator Latin American 2 Sub 610 A=0.998 G=0.002
Allele Frequency Aggregator Latin American 1 Sub 146 A=0.986 G=0.014
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
1000Genomes_30x Global Study-wide 6404 A=0.9911 G=0.0089
1000Genomes_30x African Sub 1786 A=0.9714 G=0.0286
1000Genomes_30x Europe Sub 1266 A=1.0000 G=0.0000
1000Genomes_30x South Asian Sub 1202 A=1.0000 G=0.0000
1000Genomes_30x East Asian Sub 1170 A=1.0000 G=0.0000
1000Genomes_30x American Sub 980 A=0.994 G=0.006
1000Genomes Global Study-wide 5008 A=0.9914 G=0.0086
1000Genomes African Sub 1322 A=0.9705 G=0.0295
1000Genomes East Asian Sub 1008 A=1.0000 G=0.0000
1000Genomes Europe Sub 1006 A=1.0000 G=0.0000
1000Genomes South Asian Sub 978 A=1.000 G=0.000
1000Genomes American Sub 694 A=0.994 G=0.006
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.9997 G=0.0003
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=1.0000 G=0.0000
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.999 G=0.001
Qatari Global Study-wide 216 A=0.991 G=0.009
SGDP_PRJ Global Study-wide 6 A=0.5 G=0.5
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.48438328A>G
GRCh37.p13 chr 10 NC_000010.10:g.49646371A>G
MAPK8 RefSeqGene NG_029053.2:g.136690A>G
ARHGAP22 RefSeqGene NG_053158.1:g.222938T>C
Gene: MAPK8, mitogen-activated protein kinase 8 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
MAPK8 transcript variant JNK1-b1 NM_139046.4:c.*3433= N/A 3 Prime UTR Variant
MAPK8 transcript variant 6 NM_001323320.2:c.*3299= N/A 3 Prime UTR Variant
MAPK8 transcript variant 10 NM_001323324.2:c.*3433= N/A 3 Prime UTR Variant
MAPK8 transcript variant 15 NM_001323329.2:c.*3299= N/A 3 Prime UTR Variant
MAPK8 transcript variant 11 NM_001323325.2:c.*3433= N/A 3 Prime UTR Variant
MAPK8 transcript variant 7 NM_001323321.2:c.*3433= N/A 3 Prime UTR Variant
MAPK8 transcript variant 13 NM_001323327.2:c.*3433= N/A 3 Prime UTR Variant
MAPK8 transcript variant JNK1-a1 NM_001323302.2:c.*3433= N/A 3 Prime UTR Variant
MAPK8 transcript variant JNK1-a2 NM_139049.4:c.*3299= N/A 3 Prime UTR Variant
MAPK8 transcript variant 14 NM_001323328.2:c.*3299= N/A 3 Prime UTR Variant
MAPK8 transcript variant 8 NM_001323322.2:c.*3299= N/A 3 Prime UTR Variant
MAPK8 transcript variant 17 NM_001323331.2:c.*3299= N/A 3 Prime UTR Variant
MAPK8 transcript variant 9 NM_001323323.2:c.*3299= N/A 3 Prime UTR Variant
MAPK8 transcript variant 12 NM_001323326.2:c.*3433= N/A 3 Prime UTR Variant
MAPK8 transcript variant 16 NM_001323330.2:c.*3299= N/A 3 Prime UTR Variant
MAPK8 transcript variant JNK1-b2 NM_001278547.2:c.*3299= N/A 3 Prime UTR Variant
MAPK8 transcript variant 5 NM_001278548.2:c.*3433= N/A 3 Prime UTR Variant
MAPK8 transcript variant 19 NR_136584.2:n.4773A>G N/A Non Coding Transcript Variant
MAPK8 transcript variant 18 NR_136583.2:n.4778A>G N/A Non Coding Transcript Variant
MAPK8 transcript variant 20 NR_136585.2:n.4778A>G N/A Non Coding Transcript Variant
MAPK8 transcript variant X1 XM_047425480.1:c.*3299= N/A 3 Prime UTR Variant
MAPK8 transcript variant X2 XM_024448079.2:c.*3299= N/A 3 Prime UTR Variant
MAPK8 transcript variant X3 XM_047425481.1:c.*3299= N/A 3 Prime UTR Variant
MAPK8 transcript variant X4 XM_024448080.2:c.*3433= N/A 3 Prime UTR Variant
MAPK8 transcript variant X5 XM_047425482.1:c.*3433= N/A 3 Prime UTR Variant
MAPK8 transcript variant X6 XM_047425484.1:c.*3433= N/A 3 Prime UTR Variant
Gene: ARHGAP22, Rho GTPase activating protein 22 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
ARHGAP22 transcript variant 1 NM_001256024.2:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant 2 NM_001256025.3:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant 4 NM_001256026.2:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant 7 NM_001347735.2:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant 8 NM_001347736.2:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant 9 NM_001347737.2:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant 10 NM_001347738.2:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant 3 NM_021226.4:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant 6 NR_045675.2:n. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant 11 NR_144642.2:n. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant 12 NR_144643.2:n. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant 13 NR_144644.2:n. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant 14 NR_144645.2:n. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant 15 NR_144646.2:n. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X15 XM_011540013.4:c.1055-774…

XM_011540013.4:c.1055-7746T>C

N/A Intron Variant
ARHGAP22 transcript variant X19 XM_017016476.2:c.989-7746…

XM_017016476.2:c.989-7746T>C

N/A Intron Variant
ARHGAP22 transcript variant X17 XM_024448100.2:c.1007-774…

XM_024448100.2:c.1007-7746T>C

N/A Intron Variant
ARHGAP22 transcript variant X8 XM_005270014.4:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X1 XM_011540002.3:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X3 XM_011540003.2:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X6 XM_011540005.2:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X7 XM_011540006.3:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X13 XM_011540011.3:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X20 XM_011540015.4:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X14 XM_017016471.3:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X2 XM_024448099.2:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X22 XM_024448102.2:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X24 XM_024448106.2:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X4 XM_047425586.1:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X5 XM_047425587.1:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X9 XM_047425588.1:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X10 XM_047425589.1:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X11 XM_047425590.1:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X12 XM_047425591.1:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X16 XM_047425592.1:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X18 XM_047425593.1:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X21 XM_047425594.1:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X23 XM_047425595.1:c. N/A Genic Downstream 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
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
GRCh38.p14 chr 10 NC_000010.11:g.48438328= NC_000010.11:g.48438328A>G
GRCh37.p13 chr 10 NC_000010.10:g.49646371= NC_000010.10:g.49646371A>G
MAPK8 RefSeqGene NG_029053.2:g.136690= NG_029053.2:g.136690A>G
MAPK8 transcript variant JNK1-b1 NM_139046.4:c.*3433= NM_139046.4:c.*3433A>G
MAPK8 transcript variant JNK1-b1 NM_139046.3:c.*3433= NM_139046.3:c.*3433A>G
MAPK8 transcript variant JNK1-b1 NM_139046.2:c.*3433= NM_139046.2:c.*3433A>G
MAPK8 transcript variant JNK1-a2 NM_139049.4:c.*3299= NM_139049.4:c.*3299A>G
MAPK8 transcript variant JNK1-a2 NM_139049.3:c.*3299= NM_139049.3:c.*3299A>G
MAPK8 transcript variant JNK1-a2 NM_139049.2:c.*3299= NM_139049.2:c.*3299A>G
MAPK8 transcript variant JNK1-a1 NM_001323302.2:c.*3433= NM_001323302.2:c.*3433A>G
MAPK8 transcript variant JNK1-a1 NM_001323302.1:c.*3433= NM_001323302.1:c.*3433A>G
MAPK8 transcript variant 8 NM_001323322.2:c.*3299= NM_001323322.2:c.*3299A>G
MAPK8 transcript variant 8 NM_001323322.1:c.*3299= NM_001323322.1:c.*3299A>G
MAPK8 transcript variant 13 NM_001323327.2:c.*3433= NM_001323327.2:c.*3433A>G
MAPK8 transcript variant 13 NM_001323327.1:c.*3433= NM_001323327.1:c.*3433A>G
MAPK8 transcript variant 11 NM_001323325.2:c.*3433= NM_001323325.2:c.*3433A>G
MAPK8 transcript variant 11 NM_001323325.1:c.*3433= NM_001323325.1:c.*3433A>G
MAPK8 transcript variant 17 NM_001323331.2:c.*3299= NM_001323331.2:c.*3299A>G
MAPK8 transcript variant 17 NM_001323331.1:c.*3299= NM_001323331.1:c.*3299A>G
MAPK8 transcript variant 16 NM_001323330.2:c.*3299= NM_001323330.2:c.*3299A>G
MAPK8 transcript variant 16 NM_001323330.1:c.*3299= NM_001323330.1:c.*3299A>G
MAPK8 transcript variant 12 NM_001323326.2:c.*3433= NM_001323326.2:c.*3433A>G
MAPK8 transcript variant 12 NM_001323326.1:c.*3433= NM_001323326.1:c.*3433A>G
MAPK8 transcript variant 14 NM_001323328.2:c.*3299= NM_001323328.2:c.*3299A>G
MAPK8 transcript variant 14 NM_001323328.1:c.*3299= NM_001323328.1:c.*3299A>G
MAPK8 transcript variant 9 NM_001323323.2:c.*3299= NM_001323323.2:c.*3299A>G
MAPK8 transcript variant 9 NM_001323323.1:c.*3299= NM_001323323.1:c.*3299A>G
MAPK8 transcript variant 5 NM_001278548.2:c.*3433= NM_001278548.2:c.*3433A>G
MAPK8 transcript variant 5 NM_001278548.1:c.*3433= NM_001278548.1:c.*3433A>G
MAPK8 transcript variant 10 NM_001323324.2:c.*3433= NM_001323324.2:c.*3433A>G
MAPK8 transcript variant 10 NM_001323324.1:c.*3433= NM_001323324.1:c.*3433A>G
MAPK8 transcript variant 7 NM_001323321.2:c.*3433= NM_001323321.2:c.*3433A>G
MAPK8 transcript variant 7 NM_001323321.1:c.*3433= NM_001323321.1:c.*3433A>G
MAPK8 transcript variant 20 NR_136585.2:n.4778= NR_136585.2:n.4778A>G
MAPK8 transcript variant 20 NR_136585.1:n.4816= NR_136585.1:n.4816A>G
MAPK8 transcript variant 18 NR_136583.2:n.4778= NR_136583.2:n.4778A>G
MAPK8 transcript variant 18 NR_136583.1:n.4816= NR_136583.1:n.4816A>G
MAPK8 transcript variant 15 NM_001323329.2:c.*3299= NM_001323329.2:c.*3299A>G
MAPK8 transcript variant 15 NM_001323329.1:c.*3299= NM_001323329.1:c.*3299A>G
MAPK8 transcript variant JNK1-b2 NM_001278547.2:c.*3299= NM_001278547.2:c.*3299A>G
MAPK8 transcript variant JNK1-b2 NM_001278547.1:c.*3299= NM_001278547.1:c.*3299A>G
MAPK8 transcript variant 19 NR_136584.2:n.4773= NR_136584.2:n.4773A>G
MAPK8 transcript variant 19 NR_136584.1:n.4811= NR_136584.1:n.4811A>G
MAPK8 transcript variant 6 NM_001323320.2:c.*3299= NM_001323320.2:c.*3299A>G
MAPK8 transcript variant 6 NM_001323320.1:c.*3299= NM_001323320.1:c.*3299A>G
ARHGAP22 RefSeqGene NG_053158.1:g.222938= NG_053158.1:g.222938T>C
MAPK8 transcript variant JNK1-a1 NM_002750.3:c.*3433= NM_002750.3:c.*3433A>G
MAPK8 transcript variant X2 XM_024448079.2:c.*3299= XM_024448079.2:c.*3299A>G
MAPK8 transcript variant X4 XM_024448080.2:c.*3433= XM_024448080.2:c.*3433A>G
MAPK8 transcript variant X3 XM_047425481.1:c.*3299= XM_047425481.1:c.*3299A>G
MAPK8 transcript variant X5 XM_047425482.1:c.*3433= XM_047425482.1:c.*3433A>G
MAPK8 transcript variant X1 XM_047425480.1:c.*3299= XM_047425480.1:c.*3299A>G
MAPK8 transcript variant X6 XM_047425484.1:c.*3433= XM_047425484.1:c.*3433A>G
ARHGAP22 transcript variant X15 XM_011540013.4:c.1055-7746= XM_011540013.4:c.1055-7746T>C
ARHGAP22 transcript variant X19 XM_017016476.2:c.989-7746= XM_017016476.2:c.989-7746T>C
ARHGAP22 transcript variant X17 XM_024448100.2:c.1007-7746= XM_024448100.2:c.1007-7746T>C
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, 10 Frequency submissions
No Submitter Submission ID Date (Build)
1 1000GENOMES ss224703666 Jul 14, 2010 (132)
2 EVA-GONL ss987452651 Aug 21, 2014 (142)
3 1000GENOMES ss1337308238 Aug 21, 2014 (142)
4 EVA_UK10K_ALSPAC ss1624502193 Apr 01, 2015 (144)
5 EVA_UK10K_TWINSUK ss1667496226 Apr 01, 2015 (144)
6 WEILL_CORNELL_DGM ss1930809986 Feb 12, 2016 (147)
7 HUMAN_LONGEVITY ss2174519403 Dec 20, 2016 (150)
8 GNOMAD ss2888419192 Nov 08, 2017 (151)
9 KHV_HUMAN_GENOMES ss3813435478 Jul 13, 2019 (153)
10 EVA ss3832104463 Apr 26, 2020 (154)
11 SGDP_PRJ ss3874131775 Apr 26, 2020 (154)
12 TOPMED ss4851347734 Apr 27, 2021 (155)
13 1000G_HIGH_COVERAGE ss5283929617 Oct 16, 2022 (156)
14 EVA ss5393254769 Oct 16, 2022 (156)
15 HUGCELL_USP ss5479526834 Oct 16, 2022 (156)
16 1000G_HIGH_COVERAGE ss5577811702 Oct 16, 2022 (156)
17 SANFORD_IMAGENETICS ss5649214353 Oct 16, 2022 (156)
18 EVA ss5878777461 Oct 16, 2022 (156)
19 EVA ss5940483301 Oct 16, 2022 (156)
20 1000Genomes NC_000010.10 - 49646371 Oct 12, 2018 (152)
21 1000Genomes_30x NC_000010.11 - 48438328 Oct 16, 2022 (156)
22 The Avon Longitudinal Study of Parents and Children NC_000010.10 - 49646371 Oct 12, 2018 (152)
23 gnomAD - Genomes NC_000010.11 - 48438328 Apr 27, 2021 (155)
24 Genome of the Netherlands Release 5 NC_000010.10 - 49646371 Apr 26, 2020 (154)
25 Qatari NC_000010.10 - 49646371 Apr 26, 2020 (154)
26 SGDP_PRJ NC_000010.10 - 49646371 Apr 26, 2020 (154)
27 TopMed NC_000010.11 - 48438328 Apr 27, 2021 (155)
28 UK 10K study - Twins NC_000010.10 - 49646371 Oct 12, 2018 (152)
29 ALFA NC_000010.11 - 48438328 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
49690823, 27582827, 12297708, 12851916, 26148755, 27582827, ss224703666, ss987452651, ss1337308238, ss1624502193, ss1667496226, ss1930809986, ss2888419192, ss3832104463, ss3874131775, ss5393254769, ss5649214353, ss5940483301 NC_000010.10:49646370:A:G NC_000010.11:48438327:A:G (self)
65337637, 351329480, 66893389, 5070640634, ss2174519403, ss3813435478, ss4851347734, ss5283929617, ss5479526834, ss5577811702, ss5878777461 NC_000010.11:48438327:A:G NC_000010.11:48438327: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.

No publications for rs75124279

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