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rs140600746

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs140600746(A;T)
Make rs140600746(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position49435481
GeneMUT
is asnp
is mentioned by
dbSNPrs140600746
ebirs140600746
HLIrs140600746
Exacrs140600746
Varsomers140600746
Maprs140600746
PheGenIrs140600746
hapmaprs140600746
1000 genomesrs140600746
hgdprs140600746
ensemblrs140600746
gopubmedrs140600746
geneviewrs140600746
scholarrs140600746
googlers140600746
pharmgkbrs140600746
gwascentralrs140600746
openSNPrs140600746
23andMers140600746
23andMe allrs140600746
SNP Nexus

SNPshotrs140600746
SNPdbers140600746
MSV3drs140600746
GWAS Ctlgrs140600746
Max Magnitude0
ClinVar
Risk rs140600746(T;T)
Alt rs140600746(T;T)
Reference rs140600746(A;A)
Significance Pathogenic
Disease Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
Variation info
Gene MUT
CLNDBN Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
Reversed 0
HGVS NC_000006.11:g.49403194A>T
CLNSRC
CLNACC RCV000203324.1,