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rs387907022

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907022(A;A)
Make rs387907022(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position46353829
GeneTRMU
is asnp
is mentioned by
dbSNPrs387907022
ebirs387907022
HLIrs387907022
Exacrs387907022
Varsomers387907022
Maprs387907022
PheGenIrs387907022
hapmaprs387907022
1000 genomesrs387907022
hgdprs387907022
ensemblrs387907022
gopubmedrs387907022
geneviewrs387907022
scholarrs387907022
googlers387907022
pharmgkbrs387907022
gwascentralrs387907022
openSNPrs387907022
23andMers387907022
23andMe allrs387907022
SNP Nexus

SNPshotrs387907022
SNPdbers387907022
MSV3drs387907022
GWAS Ctlgrs387907022
Max Magnitude0
ClinVar
Risk rs387907022(A;A)
Alt rs387907022(A;A)
Reference rs387907022(G;G)
Significance Pathogenic
Disease Liver failure acute infantile
Variation info
Gene TRMU
CLNDBN Liver failure acute infantile
Reversed 0
HGVS NC_000022.10:g.46749726G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023804.2,