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rs56398830

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs56398830(A;A)
Make rs56398830(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position103049340
GeneSLC10A2
is asnp
is mentioned by
dbSNPrs56398830
ClinGenrs56398830
ebirs56398830
HLIrs56398830
Exacrs56398830
Varsomers56398830
Maprs56398830
PheGenIrs56398830
hapmaprs56398830
1000 genomesrs56398830
hgdprs56398830
ensemblrs56398830
gopubmedrs56398830
geneviewrs56398830
scholarrs56398830
googlers56398830
pharmgkbrs56398830
gwascentralrs56398830
openSNPrs56398830
23andMers56398830
23andMe allrs56398830
SNP Nexus

SNPshotrs56398830
SNPdbers56398830
MSV3drs56398830
GWAS Ctlgrs56398830
GMAF0.0101
Max Magnitude0
OMIM601295
DescSOLUTE CARRIER FAMILY 10 (SODIUM/BILE ACID COTRANSPORTER FAMILY),
Variant
Relatedalso
[PMID 19823678OA-icon.png] A variant of the SLC10A2 gene encoding the apical sodium-dependent bile acid transporter is a risk factor for gallstone disease.