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rs779939886

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs779939886(A;A)
Make rs779939886(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position145646157
GeneMMAA
is asnp
is mentioned by
dbSNPrs779939886
ebirs779939886
HLIrs779939886
Exacrs779939886
Varsomers779939886
Maprs779939886
PheGenIrs779939886
hapmaprs779939886
1000 genomesrs779939886
hgdprs779939886
ensemblrs779939886
gopubmedrs779939886
geneviewrs779939886
scholarrs779939886
googlers779939886
pharmgkbrs779939886
gwascentralrs779939886
openSNPrs779939886
23andMers779939886
23andMe allrs779939886
SNP Nexus

SNPshotrs779939886
SNPdbers779939886
MSV3drs779939886
GWAS Ctlgrs779939886
Max Magnitude0
ClinVar
Risk rs779939886(A;A)
Alt rs779939886(A;A)
Reference rs779939886(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.146567309G>A
CLNSRC
CLNACC RCV000203316.1,