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rs369296618

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs369296618(A;A)
Make rs369296618(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position109557081
GeneMMAB
is asnp
is mentioned by
dbSNPrs369296618
ebirs369296618
HLIrs369296618
Exacrs369296618
Varsomers369296618
Maprs369296618
PheGenIrs369296618
hapmaprs369296618
1000 genomesrs369296618
hgdprs369296618
ensemblrs369296618
gopubmedrs369296618
geneviewrs369296618
scholarrs369296618
googlers369296618
pharmgkbrs369296618
gwascentralrs369296618
openSNPrs369296618
23andMers369296618
23andMe allrs369296618
SNP Nexus

SNPshotrs369296618
SNPdbers369296618
MSV3drs369296618
GWAS Ctlgrs369296618
Max Magnitude0
ClinVar
Risk rs369296618(A;A)
Alt rs369296618(A;A)
Reference rs369296618(G;G)
Significance Pathogenic
Disease not provided Methylmalonic aciduria cblB type
Variation info
Gene MMAB
CLNDBN not provided Methylmalonic aciduria cblB type
Reversed 0
HGVS NC_000012.11:g.109994886G>A
CLNSRC
CLNACC RCV000186019.1, RCV000190603.1,