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rs34946978

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs34946978(C;T)
Make rs34946978(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position233768226
GeneUGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs34946978
ebirs34946978
HLIrs34946978
Exacrs34946978
Varsomers34946978
Maprs34946978
PheGenIrs34946978
hapmaprs34946978
1000 genomesrs34946978
hgdprs34946978
ensemblrs34946978
gopubmedrs34946978
geneviewrs34946978
scholarrs34946978
googlers34946978
pharmgkbrs34946978
gwascentralrs34946978
openSNPrs34946978
23andMers34946978
23andMe allrs34946978
SNP Nexus

SNPshotrs34946978
SNPdbers34946978
MSV3drs34946978
GWAS Ctlgrs34946978
Max Magnitude0
ClinVar
Risk rs34946978(T;T)
Alt rs34946978(T;T)
Reference rs34946978(C;C)
Significance Probable-Pathogenic
Disease Hyperbilirubinemia
Variation info
Gene UGT1A5 UGT1A3 UGT1A9 UGT1A6 UGT1A4 UGT1A1 UGT1A10 UGT1A8 UGT1A7
CLNDBN Hyperbilirubinemia
Reversed 0
HGVS NC_000002.11:g.234676872C>T
CLNSRC
CLNACC RCV000194762.1,