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rs864309511

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864309511(A;A)
Make rs864309511(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position109568770
GeneMMAB
is asnp
is mentioned by
dbSNPrs864309511
ebirs864309511
HLIrs864309511
Exacrs864309511
Varsomers864309511
Maprs864309511
PheGenIrs864309511
hapmaprs864309511
1000 genomesrs864309511
hgdprs864309511
ensemblrs864309511
gopubmedrs864309511
geneviewrs864309511
scholarrs864309511
googlers864309511
pharmgkbrs864309511
gwascentralrs864309511
openSNPrs864309511
23andMers864309511
23andMe allrs864309511
SNP Nexus

SNPshotrs864309511
SNPdbers864309511
MSV3drs864309511
GWAS Ctlgrs864309511
Max Magnitude0
ClinVar
Risk rs864309511(A;A)
Alt rs864309511(A;A)
Reference rs864309511(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.110006575C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000202589.2,