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rs864309739

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864309739(G;G)
Make rs864309739(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position49435526
GeneMUT
is asnp
is mentioned by
dbSNPrs864309739
ebirs864309739
HLIrs864309739
Exacrs864309739
Varsomers864309739
Maprs864309739
PheGenIrs864309739
hapmaprs864309739
1000 genomesrs864309739
hgdprs864309739
ensemblrs864309739
gopubmedrs864309739
geneviewrs864309739
scholarrs864309739
googlers864309739
pharmgkbrs864309739
gwascentralrs864309739
openSNPrs864309739
23andMers864309739
23andMe allrs864309739
SNP Nexus

SNPshotrs864309739
SNPdbers864309739
MSV3drs864309739
GWAS Ctlgrs864309739
Max Magnitude0
ClinVar
Risk rs864309739(G;G)
Alt rs864309739(G;G)
Reference rs864309739(T;T)
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 1
HGVS NC_000006.11:g.49403239A>C
CLNSRC
CLNACC RCV000203365.1,