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rs62625011

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs62625011(A;A)
Make rs62625011(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position233767092
GeneUGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs62625011
ebirs62625011
HLIrs62625011
Exacrs62625011
Varsomers62625011
Maprs62625011
PheGenIrs62625011
hapmaprs62625011
1000 genomesrs62625011
hgdprs62625011
ensemblrs62625011
gopubmedrs62625011
geneviewrs62625011
scholarrs62625011
googlers62625011
pharmgkbrs62625011
gwascentralrs62625011
openSNPrs62625011
23andMers62625011
23andMe allrs62625011
SNP Nexus

SNPshotrs62625011
SNPdbers62625011
MSV3drs62625011
GWAS Ctlgrs62625011
Max Magnitude0
ClinVar
Risk rs62625011(A;A)
Alt rs62625011(A;A)
Reference rs62625011(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.234675738G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013060.24,