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rs17680137

From SNPedia

Orientationplus
Stabilizedplus
Make rs17680137(C;C)
Make rs17680137(C;G)
Make rs17680137(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position20862972
GeneSLCO1B3
is asnp
is mentioned by
dbSNPrs17680137
ebirs17680137
HLIrs17680137
Exacrs17680137
Varsomers17680137
Maprs17680137
PheGenIrs17680137
hapmaprs17680137
1000 genomesrs17680137
hgdprs17680137
ensemblrs17680137
gopubmedrs17680137
geneviewrs17680137
scholarrs17680137
googlers17680137
pharmgkbrs17680137
gwascentralrs17680137
openSNPrs17680137
23andMers17680137
23andMe allrs17680137
SNP Nexus

SNPshotrs17680137
SNPdbers17680137
MSV3drs17680137
GWAS Ctlgrs17680137
GMAF0.07805
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 20639394OA-icon.png] Genome-wide association of serum bilirubin levels in Korean population
OMIM601816
Desc
Variant
Relatedalso


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


GET Evidence
rs17680137
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.101562
summary