rs56398830

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs56398830(A;A)

Make rs56398830(A;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

103049340

Gene

SLC10A2

is a	snp
is	mentioned by
dbSNP	rs56398830
dbSNP (classic)	rs56398830
ClinGen	rs56398830
ebi	rs56398830
HLI	rs56398830
Exac	rs56398830
Gnomad	rs56398830
Varsome	rs56398830
LitVar	rs56398830
Map	rs56398830
PheGenI	rs56398830
Biobank	rs56398830
1000 genomes	rs56398830
hgdp	rs56398830
ensembl	rs56398830
geneview	rs56398830
scholar	rs56398830
google	rs56398830
pharmgkb	rs56398830
gwascentral	rs56398830
openSNP	rs56398830
23andMe	rs56398830
SNPshot	rs56398830
SNPdbe	rs56398830
MSV3d	rs56398830
GWAS Ctlg	rs56398830

GMAF

0.0101

Max Magnitude

0

OMIM	601295
Desc	SOLUTE CARRIER FAMILY 10 (SODIUM/BILE ACID COTRANSPORTER FAMILY),
Variant
Related	also

[PMID 19823678] A variant of the SLC10A2 gene encoding the apical sodium-dependent bile acid transporter is a risk factor for gallstone disease.

ClinVar
Risk	rs56398830(A;A)
Alt	rs56398830(A;A)
Reference	Rs56398830(G;G)
Significance	Probable-non-pathogenic
Disease	not provided not specified
Variation	info
Gene	SLC10A2
CLNDBN	not provided not specified
Reversed	0
HGVS	NC_000013.10:g.103701690G>A
CLNSRC
CLNACC	RCV000416197.1, RCV000454501.1,