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rs2117032

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) increase of 0.096 mg/dl in bilirubin levels
(C;T) increase of 0.048 mg/dl in bilirubin levels
Make rs2117032(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position20921188
is asnp
is mentioned by
dbSNPrs2117032
ebirs2117032
HLIrs2117032
Exacrs2117032
Varsomers2117032
Maprs2117032
PheGenIrs2117032
hapmaprs2117032
1000 genomesrs2117032
hgdprs2117032
ensemblrs2117032
gopubmedrs2117032
geneviewrs2117032
scholarrs2117032
googlers2117032
pharmgkbrs2117032
gwascentralrs2117032
openSNPrs2117032
23andMers2117032
23andMe allrs2117032
SNP Nexus

SNPshotrs2117032
SNPdbers2117032
MSV3drs2117032
GWAS Ctlgrs2117032
GMAF0.4784
Max Magnitude
? (C;C) (C;T) (T;T) 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 C
P-val 3E-14
Odds Ratio 0.13 [0.08-0.18] SD increase


[PMID 20639394OA-icon.png] Genome-wide association of serum bilirubin levels in Korean population


[PMID 22580719] UGT1A1, SLCO1B1, and SLCO1B3 polymorphisms versus neonatal hyperbilirubinemia: is there an association?


GET Evidence
rs2117032
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.390625
summary