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rs2291075

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2291075(C;T)
Make rs2291075(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position21178691
GeneSLCO1B1
is asnp
is mentioned by
dbSNPrs2291075
dbSNP (classic)rs2291075
ClinGenrs2291075
ebirs2291075
HLIrs2291075
Exacrs2291075
Gnomadrs2291075
Varsomers2291075
LitVarrs2291075
Maprs2291075
PheGenIrs2291075
Biobankrs2291075
1000 genomesrs2291075
hgdprs2291075
ensemblrs2291075
geneviewrs2291075
scholarrs2291075
googlers2291075
pharmgkbrs2291075
gwascentralrs2291075
openSNPrs2291075
23andMers2291075
SNPshotrs2291075
SNPdbers2291075
MSV3drs2291075
GWAS Ctlgrs2291075
GMAF0.449
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 23970802OA-icon.png] SLCO1B1 Variants and Urine Arsenic Metabolites in the Strong Heart Family Study


[PMID 19419973OA-icon.png] Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia.


ClinVar
Risk rs2291075(T;T)
Alt rs2291075(T;T)
Reference Rs2291075(C;C)
Significance Non-pathogenic
Disease not specified Rotor syndrome
Variation info
Gene SLCO1B1
CLNDBN not specified Rotor syndrome
Reversed 0
HGVS NC_000012.11:g.21331625C>T
CLNSRC
CLNACC RCV000248856.1, RCV000260910.1,