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rs35003977

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs35003977(G;G)
Make rs35003977(G;T)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position233760961
GeneUGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs35003977
dbSNP (classic)rs35003977
ClinGenrs35003977
ebirs35003977
HLIrs35003977
Exacrs35003977
Gnomadrs35003977
Varsomers35003977
LitVarrs35003977
Maprs35003977
PheGenIrs35003977
Biobankrs35003977
1000 genomesrs35003977
hgdprs35003977
ensemblrs35003977
geneviewrs35003977
scholarrs35003977
googlers35003977
pharmgkbrs35003977
gwascentralrs35003977
openSNPrs35003977
23andMers35003977
23andMe allrs35003977
SNPshotrs35003977
SNPdbers35003977
MSV3drs35003977
GWAS Ctlgrs35003977
Max Magnitude0
ClinVar
Risk rs35003977(G;G)
Alt rs35003977(G;G)
Reference Rs35003977(T;T)
Significance Probable-Pathogenic
Disease Hyperbilirubinemia Gilbert's syndrome Crigler-Najjar syndrome Hyperbilirubinemia transient familial neonatal
Variation info
Gene UGT1A5 UGT1A9 UGT1A3 UGT1A6 UGT1A4 UGT1A1 UGT1A8 UGT1A10 UGT1A7
CLNDBN Hyperbilirubinemia Gilbert's syndrome Crigler-Najjar syndrome Hyperbilirubinemia transient familial neonatal
Reversed 0
HGVS NC_000002.11:g.234669607T>G
CLNSRC UniProtKB (protein)
CLNACC RCV000147904.1, RCV000313763.1, RCV000348706.1, RCV000396791.1,