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rs564069299

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs564069299(C;T)
Make rs564069299(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position49451692
GeneMUT
is asnp
is mentioned by
dbSNPrs564069299
ebirs564069299
HLIrs564069299
Exacrs564069299
Varsomers564069299
Maprs564069299
PheGenIrs564069299
hapmaprs564069299
1000 genomesrs564069299
hgdprs564069299
ensemblrs564069299
gopubmedrs564069299
geneviewrs564069299
scholarrs564069299
googlers564069299
pharmgkbrs564069299
gwascentralrs564069299
openSNPrs564069299
23andMers564069299
23andMe allrs564069299
SNP Nexus

SNPshotrs564069299
SNPdbers564069299
MSV3drs564069299
GWAS Ctlgrs564069299
Max Magnitude0
ClinVar
Risk rs564069299(T;T)
Alt rs564069299(T;T)
Reference rs564069299(C;C)
Significance Pathogenic
Disease not provided Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
Variation info
Gene MUT
CLNDBN not provided Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
Reversed 0
HGVS NC_000006.11:g.49419405C>T
CLNSRC
CLNACC RCV000186046.1, RCV000203318.1,