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rs864309510

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864309510(C;C)
Make rs864309510(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position109561853
GeneMMAB
is asnp
is mentioned by
dbSNPrs864309510
ebirs864309510
HLIrs864309510
Exacrs864309510
Varsomers864309510
Maprs864309510
PheGenIrs864309510
hapmaprs864309510
1000 genomesrs864309510
hgdprs864309510
ensemblrs864309510
gopubmedrs864309510
geneviewrs864309510
scholarrs864309510
googlers864309510
pharmgkbrs864309510
gwascentralrs864309510
openSNPrs864309510
23andMers864309510
23andMe allrs864309510
SNP Nexus

SNPshotrs864309510
SNPdbers864309510
MSV3drs864309510
GWAS Ctlgrs864309510
Max Magnitude0
ClinVar
Risk rs864309510(C;C)
Alt rs864309510(C;C)
Reference rs864309510(G;G)
Significance Pathogenic
Disease Methylmalonic aciduria cblB type
Variation info
Gene MMAB
CLNDBN Methylmalonic aciduria cblB type
Reversed 1
HGVS NC_000012.11:g.109999658C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000202577.2,