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rs760782399

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs760782399(G;T)
Make rs760782399(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position49457872
GeneMUT
is asnp
is mentioned by
dbSNPrs760782399
ebirs760782399
HLIrs760782399
Exacrs760782399
Varsomers760782399
Maprs760782399
PheGenIrs760782399
hapmaprs760782399
1000 genomesrs760782399
hgdprs760782399
ensemblrs760782399
gopubmedrs760782399
geneviewrs760782399
scholarrs760782399
googlers760782399
pharmgkbrs760782399
gwascentralrs760782399
openSNPrs760782399
23andMers760782399
23andMe allrs760782399
SNP Nexus

SNPshotrs760782399
SNPdbers760782399
MSV3drs760782399
GWAS Ctlgrs760782399
Max Magnitude0
ClinVar
Risk rs760782399(T;T)
Alt rs760782399(T;T)
Reference rs760782399(G;G)
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 0
HGVS NC_000006.11:g.49425585G>T
CLNSRC
CLNACC RCV000186054.1, RCV000203406.1,