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rs864309731

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 3 Carrier of a methylmalonic aciduria type cblA mutation
(G;G) 0 common in clinvar


Make rs864309731(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position145655253
GeneMMAA
is asnp
is mentioned by
dbSNPrs864309731
dbSNP (classic)rs864309731
ClinGenrs864309731
ebirs864309731
HLIrs864309731
Exacrs864309731
Gnomadrs864309731
Varsomers864309731
LitVarrs864309731
Maprs864309731
PheGenIrs864309731
Biobankrs864309731
1000 genomesrs864309731
hgdprs864309731
ensemblrs864309731
geneviewrs864309731
scholarrs864309731
googlers864309731
pharmgkbrs864309731
gwascentralrs864309731
openSNPrs864309731
23andMers864309731
SNPshotrs864309731
SNPdbers864309731
MSV3drs864309731
GWAS Ctlgrs864309731
Max Magnitude0
ClinVar
Risk rs864309731(A;A)
Alt rs864309731(A;A)
Reference Rs864309731(G;G)
Significance Pathogenic
Disease Methylmalonic aciduria cblA type
Variation info
Gene MMAA
CLNDBN Methylmalonic aciduria cblA type
Reversed 0
HGVS NC_000004.11:g.146576405G>A
CLNSRC UniProtKB (protein)
CLNACC RCV000203388.1,