rs7311358

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs7311358(A;A)

Make rs7311358(A;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

20862826

Gene

SLCO1B3

is a	snp
is	mentioned by
dbSNP	rs7311358
dbSNP (classic)	rs7311358
ClinGen	rs7311358
ebi	rs7311358
HLI	rs7311358
Exac	rs7311358
Gnomad	rs7311358
Varsome	rs7311358
LitVar	rs7311358
Map	rs7311358
PheGenI	rs7311358
Biobank	rs7311358
1000 genomes	rs7311358
hgdp	rs7311358
ensembl	rs7311358
geneview	rs7311358
scholar	rs7311358
google	rs7311358
pharmgkb	rs7311358
gwascentral	rs7311358
openSNP	rs7311358
23andMe	rs7311358
SNPshot	rs7311358
SNPdbe	rs7311358
MSV3d	rs7311358
GWAS Ctlg	rs7311358

GMAF

0.2906

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 22136368] Influence of genomic ancestry on the distribution of SLCO1B1, SLCO1B3 and ABCB1 gene polymorphisms among Brazilians.

[PMID 23133420] Pharmacogenomic Diversity among Brazilians: Influence of Ancestry, Self-Reported Color, and Geographical Origin.

ClinVar
Risk	rs7311358(A;A)
Alt	rs7311358(A;A)
Reference	Rs7311358(G;G)
Significance	Non-pathogenic
Disease	not specified Rotor syndrome
Variation	info
Gene	SLCO1B3
CLNDBN	not specified Rotor syndrome
Reversed	0
HGVS	NC_000012.11:g.21015760G>A
CLNSRC
CLNACC	RCV000253120.1, RCV000351083.1,

[PMID 30992538] Impact of SLCO1B3 polymorphisms on clinical outcomes in lung allograft recipients receiving mycophenolic acid.