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rs766314948

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs766314948(C;C)
Make rs766314948(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position46352316
GeneTRMU
is asnp
is mentioned by
dbSNPrs766314948
ebirs766314948
HLIrs766314948
Exacrs766314948
Varsomers766314948
Maprs766314948
PheGenIrs766314948
hapmaprs766314948
1000 genomesrs766314948
hgdprs766314948
ensemblrs766314948
gopubmedrs766314948
geneviewrs766314948
scholarrs766314948
googlers766314948
pharmgkbrs766314948
gwascentralrs766314948
openSNPrs766314948
23andMers766314948
23andMe allrs766314948
SNP Nexus

SNPshotrs766314948
SNPdbers766314948
MSV3drs766314948
GWAS Ctlgrs766314948
Max Magnitude0
ClinVar
Risk rs766314948(C;C)
Alt rs766314948(C;C)
Reference rs766314948(T;T)
Significance Probable-Pathogenic
Disease Liver failure acute infantile
Variation info
Gene TRMU
CLNDBN Liver failure acute infantile
Reversed 0
HGVS NC_000022.10:g.46748213T>C
CLNSRC
CLNACC RCV000196798.1,