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rs386576623

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs386576623(A;G)
Make rs386576623(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position233768333
GeneUGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs386576623
ebirs386576623
HLIrs386576623
Exacrs386576623
Varsomers386576623
Maprs386576623
PheGenIrs386576623
hapmaprs386576623
1000 genomesrs386576623
hgdprs386576623
ensemblrs386576623
gopubmedrs386576623
geneviewrs386576623
scholarrs386576623
googlers386576623
pharmgkbrs386576623
gwascentralrs386576623
openSNPrs386576623
23andMers386576623
23andMe allrs386576623
SNP Nexus

SNPshotrs386576623
SNPdbers386576623
MSV3drs386576623
GWAS Ctlgrs386576623
Max Magnitude0
ClinVar
Risk rs386576623(G;G)
Alt rs386576623(G;G)
Reference rs386576623(A;A)
Significance Pathogenic
Disease Crigler-Najjar syndrome Gilbert's syndrome
Variation info
Gene UGT1A5 UGT1A9 UGT1A3 UGT1A6 UGT1A4 UGT1A1 UGT1A8 UGT1A10 UGT1A7
CLNDBN Crigler-Najjar syndrome, type II Gilbert's syndrome
Reversed 0
HGVS NC_000002.12:g.233768333A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013079.15, RCV000013080.22,