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rs864309737

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864309737(A;G)
Make rs864309737(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position49451701
GeneMUT
is asnp
is mentioned by
dbSNPrs864309737
ebirs864309737
HLIrs864309737
Exacrs864309737
Varsomers864309737
Maprs864309737
PheGenIrs864309737
hapmaprs864309737
1000 genomesrs864309737
hgdprs864309737
ensemblrs864309737
gopubmedrs864309737
geneviewrs864309737
scholarrs864309737
googlers864309737
pharmgkbrs864309737
gwascentralrs864309737
openSNPrs864309737
23andMers864309737
23andMe allrs864309737
SNP Nexus

SNPshotrs864309737
SNPdbers864309737
MSV3drs864309737
GWAS Ctlgrs864309737
Max Magnitude0
ClinVar
Risk rs864309737(G;G)
Alt rs864309737(G;G)
Reference rs864309737(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 1
HGVS NC_000006.11:g.49419414T>C
CLNSRC
CLNACC RCV000203385.1,