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rs797046091

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs797046091(-;-)
Make rs797046091(-;AG)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position233761009
GeneUGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs797046091
dbSNP (old)rs797046091
ClinGenrs797046091
ebirs797046091
HLIrs797046091
Exacrs797046091
Gnomadrs797046091
Varsomers797046091
Maprs797046091
PheGenIrs797046091
Biobankrs797046091
1000 genomesrs797046091
hgdprs797046091
ensemblrs797046091
gopubmedrs797046091
geneviewrs797046091
scholarrs797046091
googlers797046091
pharmgkbrs797046091
gwascentralrs797046091
openSNPrs797046091
23andMers797046091
23andMe allrs797046091
SNP Nexus

SNPshotrs797046091
SNPdbers797046091
MSV3drs797046091
GWAS Ctlgrs797046091
Max Magnitude0
ClinVar
Risk rs797046091(-;-)
Alt rs797046091(-;-)
Reference Rs797046091(AG;AG)
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.234669655_234669656delAG
CLNSRC
CLNACC RCV000194838.1,