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rs147401037

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs147401037(G;G)
Make rs147401037(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position71124406
GeneMCEE
is asnp
is mentioned by
dbSNPrs147401037
ebirs147401037
HLIrs147401037
Exacrs147401037
Varsomers147401037
Maprs147401037
PheGenIrs147401037
hapmaprs147401037
1000 genomesrs147401037
hgdprs147401037
ensemblrs147401037
gopubmedrs147401037
geneviewrs147401037
scholarrs147401037
googlers147401037
pharmgkbrs147401037
gwascentralrs147401037
openSNPrs147401037
23andMers147401037
23andMe allrs147401037
SNP Nexus

SNPshotrs147401037
SNPdbers147401037
MSV3drs147401037
GWAS Ctlgrs147401037
Max Magnitude0
ClinVar
Risk rs147401037(G;G)
Alt rs147401037(G;G)
Reference rs147401037(T;T)
Significance Pathogenic
Disease not provided Methylmalonyl-CoA epimerase deficiency
Variation info
Gene MCEE
CLNDBN not provided Methylmalonyl-CoA epimerase deficiency
Reversed 0
HGVS NC_000002.11:g.71351536T>G
CLNSRC
CLNACC RCV000186009.2, RCV000203363.1,