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rs35648932

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs35648932(C;T)
Make rs35648932(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position109561798
GeneMMAB
is asnp
is mentioned by
dbSNPrs35648932
ebirs35648932
HLIrs35648932
Exacrs35648932
Varsomers35648932
Maprs35648932
PheGenIrs35648932
hapmaprs35648932
1000 genomesrs35648932
hgdprs35648932
ensemblrs35648932
gopubmedrs35648932
geneviewrs35648932
scholarrs35648932
googlers35648932
pharmgkbrs35648932
gwascentralrs35648932
openSNPrs35648932
23andMers35648932
23andMe allrs35648932
SNP Nexus

SNPshotrs35648932
SNPdbers35648932
MSV3drs35648932
GWAS Ctlgrs35648932
Max Magnitude0
ClinVar
Risk rs35648932(T;T)
Alt rs35648932(T;T)
Reference rs35648932(C;C)
Significance Pathogenic
Disease Methylmalonic aciduria cblB type
Variation info
Gene MMAB
CLNDBN Methylmalonic aciduria cblB type
Reversed 0
HGVS NC_000012.11:g.109999603C>T
CLNSRC
CLNACC RCV000203394.1,