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rs398123276

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123276(A;G)
Make rs398123276(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position49447787
GeneMUT
is asnp
is mentioned by
dbSNPrs398123276
ebirs398123276
HLIrs398123276
Exacrs398123276
Varsomers398123276
Maprs398123276
PheGenIrs398123276
hapmaprs398123276
1000 genomesrs398123276
hgdprs398123276
ensemblrs398123276
gopubmedrs398123276
geneviewrs398123276
scholarrs398123276
googlers398123276
pharmgkbrs398123276
gwascentralrs398123276
openSNPrs398123276
23andMers398123276
23andMe allrs398123276
SNP Nexus

SNPshotrs398123276
SNPdbers398123276
MSV3drs398123276
GWAS Ctlgrs398123276
Max Magnitude0
ClinVar
Risk rs398123276(G;G)
Alt rs398123276(G;G)
Reference rs398123276(A;A)
Significance Pathogenic
Disease not provided Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
Variation info
Gene MUT
CLNDBN not provided Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
Reversed 1
HGVS NC_000006.11:g.49415500T>C
CLNSRC ClinVar
CLNACC RCV000078438.3, RCV000180117.1,