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rs766420

From SNPedia

Orientationminus
Stabilizedminus
Make rs766420(C;C)
Make rs766420(C;G)
Make rs766420(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154326058
GeneTKTL1
is asnp
is mentioned by
dbSNPrs766420
ebirs766420
HLIrs766420
Exacrs766420
Varsomers766420
Maprs766420
PheGenIrs766420
hapmaprs766420
1000 genomesrs766420
hgdprs766420
ensemblrs766420
gopubmedrs766420
geneviewrs766420
scholarrs766420
googlers766420
pharmgkbrs766420
gwascentralrs766420
openSNPrs766420
23andMers766420
23andMe allrs766420
SNP Nexus

SNPshotrs766420
SNPdbers766420
MSV3drs766420
GWAS Ctlgrs766420
GMAF0.3071
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 19419973OA-icon.png]
Trait Bilirubin levels
Title Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia
Risk Allele G
P-val 9E-9
Odds Ratio 0.18 [0.12-0.24] SD decrease



GET Evidence
rs766420
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.347826
summary