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rs35350960

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs35350960(A;A)
Make rs35350960(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position233760973
GeneUGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs35350960
ebirs35350960
HLIrs35350960
Exacrs35350960
Varsomers35350960
Maprs35350960
PheGenIrs35350960
hapmaprs35350960
1000 genomesrs35350960
hgdprs35350960
ensemblrs35350960
gopubmedrs35350960
geneviewrs35350960
scholarrs35350960
googlers35350960
pharmgkbrs35350960
gwascentralrs35350960
openSNPrs35350960
23andMers35350960
23andMe allrs35350960
SNP Nexus

SNPshotrs35350960
SNPdbers35350960
MSV3drs35350960
GWAS Ctlgrs35350960
GMAF0.0004591
Max Magnitude0
OMIM191740
Desc
Variant0010
Relatedalso


ClinVar
Risk rs35350960(A,T;A,T)
Alt rs35350960(A,T;A,T)
Reference rs35350960(C;C)
Significance Other
Disease Gilbert's syndrome Crigler-Najjar syndrome not specified
Variation info
Gene UGT1A5 UGT1A9 UGT1A3 UGT1A6 UGT1A4 UGT1A1 UGT1A8 UGT1A10 UGT1A7
CLNDBN Gilbert's syndrome Crigler-Najjar syndrome, type II not specified
Reversed 0
HGVS NC_000002.11:g.234669619C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013062.23, RCV000013063.24, RCV000147905.1,



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