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rs864309509

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864309509(C;C)
Make rs864309509(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position109568773
GeneMMAB
is asnp
is mentioned by
dbSNPrs864309509
ebirs864309509
HLIrs864309509
Exacrs864309509
Varsomers864309509
Maprs864309509
PheGenIrs864309509
hapmaprs864309509
1000 genomesrs864309509
hgdprs864309509
ensemblrs864309509
gopubmedrs864309509
geneviewrs864309509
scholarrs864309509
googlers864309509
pharmgkbrs864309509
gwascentralrs864309509
openSNPrs864309509
23andMers864309509
23andMe allrs864309509
SNP Nexus

SNPshotrs864309509
SNPdbers864309509
MSV3drs864309509
GWAS Ctlgrs864309509
Max Magnitude0
ClinVar
Risk rs864309509(C;C)
Alt rs864309509(C;C)
Reference rs864309509(T;T)
Significance Pathogenic
Disease Methylmalonic aciduria cblB type
Variation info
Gene MMAB
CLNDBN Methylmalonic aciduria cblB type
Reversed 1
HGVS NC_000012.11:g.110006578A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000202588.2,