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rs71581941

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs71581941(C;T)
Make rs71581941(T;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position21222355
GeneSLCO1B1
is asnp
is mentioned by
dbSNPrs71581941
ebirs71581941
HLIrs71581941
Exacrs71581941
Varsomers71581941
Maprs71581941
PheGenIrs71581941
hapmaprs71581941
1000 genomesrs71581941
hgdprs71581941
ensemblrs71581941
gopubmedrs71581941
geneviewrs71581941
scholarrs71581941
googlers71581941
pharmgkbrs71581941
gwascentralrs71581941
openSNPrs71581941
23andMers71581941
23andMe allrs71581941
SNP Nexus

SNPshotrs71581941
SNPdbers71581941
MSV3drs71581941
GWAS Ctlgrs71581941
Max Magnitude0


ClinVar
Risk rs71581941(A,T;A,T)
Alt rs71581941(A,T;A,T)
Reference rs71581941(C;C)
Significance Pathogenic
Disease Rotor syndrome
Variation info
Gene SLCO1B1
CLNDBN Rotor syndrome
Reversed 0
HGVS NC_000012.11:g.21375289C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023390.2,