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rs797046090

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797046090(-;GTAC)
Make rs797046090(GTAC;GTAC)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position233760525
GeneUGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs797046090
ClinGenrs797046090
ebirs797046090
HLIrs797046090
Exacrs797046090
Varsomers797046090
Maprs797046090
PheGenIrs797046090
hapmaprs797046090
1000 genomesrs797046090
hgdprs797046090
ensemblrs797046090
gopubmedrs797046090
geneviewrs797046090
scholarrs797046090
googlers797046090
pharmgkbrs797046090
gwascentralrs797046090
openSNPrs797046090
23andMers797046090
23andMe allrs797046090
SNP Nexus

SNPshotrs797046090
SNPdbers797046090
MSV3drs797046090
GWAS Ctlgrs797046090
Max Magnitude0
ClinVar
Risk rs797046090(CGTA;CGTA)
Alt rs797046090(CGTA;CGTA)
Reference Rs797046090(-;-)
Significance Pathogenic
Disease Hyperbilirubinemia
Variation info
Gene UGT1A5 UGT1A3 UGT1A9 UGT1A6 UGT1A4 UGT1A1 UGT1A8 UGT1A10 UGT1A7
CLNDBN Hyperbilirubinemia
Reversed 0
HGVS NC_000002.11:g.234669171_234669172insGTAC
CLNSRC
CLNACC RCV000193803.1,