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rs118203991

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs118203991(A;A)
Make rs118203991(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position46353809
GeneTRMU
is asnp
is mentioned by
dbSNPrs118203991
ebirs118203991
HLIrs118203991
Exacrs118203991
Varsomers118203991
Maprs118203991
PheGenIrs118203991
hapmaprs118203991
1000 genomesrs118203991
hgdprs118203991
ensemblrs118203991
gopubmedrs118203991
geneviewrs118203991
scholarrs118203991
googlers118203991
pharmgkbrs118203991
gwascentralrs118203991
openSNPrs118203991
23andMers118203991
23andMe allrs118203991
SNP Nexus

SNPshotrs118203991
SNPdbers118203991
MSV3drs118203991
GWAS Ctlgrs118203991
Max Magnitude0
OMIM610230
Desc
Variant0004
Relatedalso
ClinVar
Risk rs118203991(A;A)
Alt rs118203991(A;A)
Reference rs118203991(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.46749706G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001356.2,