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rs587776763

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776763(-;-)
Make rs587776763(-;T)
Make rs587776763(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position233760761
GeneUGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs587776763
ebirs587776763
HLIrs587776763
Exacrs587776763
Varsomers587776763
Maprs587776763
PheGenIrs587776763
hapmaprs587776763
1000 genomesrs587776763
hgdprs587776763
ensemblrs587776763
gopubmedrs587776763
geneviewrs587776763
scholarrs587776763
googlers587776763
pharmgkbrs587776763
gwascentralrs587776763
openSNPrs587776763
23andMers587776763
23andMe allrs587776763
SNP Nexus

SNPshotrs587776763
SNPdbers587776763
MSV3drs587776763
GWAS Ctlgrs587776763
Max Magnitude0
ClinVar
Risk rs587776763(T;T)
Alt rs587776763(T;T)
Reference rs587776763(;)
Significance Pathogenic
Disease Crigler Najjar syndrome
Variation info
Gene UGT1A5 UGT1A9 UGT1A3 UGT1A6 UGT1A4 UGT1A1 UGT1A8 UGT1A10 UGT1A7
CLNDBN Crigler Najjar syndrome, type 1
Reversed 0
HGVS NC_000002.11:g.234669407_234669408insT
CLNSRC OMIM Allelic Variant
CLNACC RCV000013067.16,