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rs587776764

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776764(C;C)
Make rs587776764(C;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position233761152
GeneUGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs587776764
ebirs587776764
HLIrs587776764
Exacrs587776764
Varsomers587776764
Maprs587776764
PheGenIrs587776764
hapmaprs587776764
1000 genomesrs587776764
hgdprs587776764
ensemblrs587776764
gopubmedrs587776764
geneviewrs587776764
scholarrs587776764
googlers587776764
pharmgkbrs587776764
gwascentralrs587776764
openSNPrs587776764
23andMers587776764
23andMe allrs587776764
SNP Nexus

SNPshotrs587776764
SNPdbers587776764
MSV3drs587776764
GWAS Ctlgrs587776764
Max Magnitude0
ClinVar
Risk rs587776764(C;C)
Alt rs587776764(C;C)
Reference rs587776764(G;G)
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.234669798G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013068.24,