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rs587776766

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587776766(A;G)
Make rs587776766(G;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position233768218
GeneUGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs587776766
ebirs587776766
HLIrs587776766
Exacrs587776766
Varsomers587776766
Maprs587776766
PheGenIrs587776766
hapmaprs587776766
1000 genomesrs587776766
hgdprs587776766
ensemblrs587776766
gopubmedrs587776766
geneviewrs587776766
scholarrs587776766
googlers587776766
pharmgkbrs587776766
gwascentralrs587776766
openSNPrs587776766
23andMers587776766
23andMe allrs587776766
SNP Nexus

SNPshotrs587776766
SNPdbers587776766
MSV3drs587776766
GWAS Ctlgrs587776766
Max Magnitude0
ClinVar
Risk rs587776766(G;G)
Alt rs587776766(G;G)
Reference rs587776766(A;A)
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.234676864A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013070.23,