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rs199971687

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199971687(C;T)
Make rs199971687(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position109565177
GeneMMAB
is asnp
is mentioned by
dbSNPrs199971687
ebirs199971687
HLIrs199971687
Exacrs199971687
Varsomers199971687
Maprs199971687
PheGenIrs199971687
hapmaprs199971687
1000 genomesrs199971687
hgdprs199971687
ensemblrs199971687
gopubmedrs199971687
geneviewrs199971687
scholarrs199971687
googlers199971687
pharmgkbrs199971687
gwascentralrs199971687
openSNPrs199971687
23andMers199971687
23andMe allrs199971687
SNP Nexus

SNPshotrs199971687
SNPdbers199971687
MSV3drs199971687
GWAS Ctlgrs199971687
Max Magnitude0
ClinVar
Risk rs199971687(T;T)
Alt rs199971687(T;T)
Reference rs199971687(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.110002982C>T
CLNSRC
CLNACC RCV000203348.1,