Have questions? Visit https://www.reddit.com/r/SNPedia

rs7311358

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs7311358(A;A)
Make rs7311358(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position20862826
GeneSLCO1B3
is asnp
is mentioned by
dbSNPrs7311358
dbSNP (classic)rs7311358
ClinGenrs7311358
ebirs7311358
HLIrs7311358
Exacrs7311358
Gnomadrs7311358
Varsomers7311358
LitVarrs7311358
Maprs7311358
PheGenIrs7311358
Biobankrs7311358
1000 genomesrs7311358
hgdprs7311358
ensemblrs7311358
geneviewrs7311358
scholarrs7311358
googlers7311358
pharmgkbrs7311358
gwascentralrs7311358
openSNPrs7311358
23andMers7311358
23andMe allrs7311358
SNPshotrs7311358
SNPdbers7311358
MSV3drs7311358
GWAS Ctlgrs7311358
GMAF0.2906
Max Magnitude0
? (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 23133420OA-icon.png] 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.