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rs587784535

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784535(G;T)
Make rs587784535(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position233767937
GeneUGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs587784535
ebirs587784535
HLIrs587784535
Exacrs587784535
Varsomers587784535
Maprs587784535
PheGenIrs587784535
hapmaprs587784535
1000 genomesrs587784535
hgdprs587784535
ensemblrs587784535
gopubmedrs587784535
geneviewrs587784535
scholarrs587784535
googlers587784535
pharmgkbrs587784535
gwascentralrs587784535
openSNPrs587784535
23andMers587784535
23andMe allrs587784535
SNP Nexus

SNPshotrs587784535
SNPdbers587784535
MSV3drs587784535
GWAS Ctlgrs587784535
Max Magnitude0
ClinVar
Risk rs587784535(T;T)
Alt rs587784535(T;T)
Reference rs587784535(G;G)
Significance Pathogenic
Disease Hyperbilirubinemia
Variation info
Gene UGT1A5 UGT1A9 UGT1A3 UGT1A6 UGT1A4 UGT1A1 UGT1A8 UGT1A10 UGT1A7
CLNDBN Hyperbilirubinemia
Reversed 0
HGVS NC_000002.11:g.234676583G>T
CLNSRC
CLNACC RCV000147893.1,