Have questions? Visit https://www.reddit.com/r/SNPedia

rs121434277

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434277(A;A)
Make rs121434277(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position75734850
GeneACADM
is asnp
is mentioned by
dbSNPrs121434277
ebirs121434277
HLIrs121434277
Exacrs121434277
Varsomers121434277
Maprs121434277
PheGenIrs121434277
hapmaprs121434277
1000 genomesrs121434277
hgdprs121434277
ensemblrs121434277
gopubmedrs121434277
geneviewrs121434277
scholarrs121434277
googlers121434277
pharmgkbrs121434277
gwascentralrs121434277
openSNPrs121434277
23andMers121434277
23andMe allrs121434277
SNP Nexus

SNPshotrs121434277
SNPdbers121434277
MSV3drs121434277
GWAS Ctlgrs121434277
Max Magnitude0
OMIM607008
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121434277(A,T;A,T)
Alt rs121434277(A,T;A,T)
Reference rs121434277(G;G)
Significance Pathogenic
Disease Medium-chain acyl-coenzyme A dehydrogenase deficiency
Variation info
Gene ACADM
CLNDBN Medium-chain acyl-coenzyme A dehydrogenase deficiency
Reversed 0
HGVS NC_000001.10:g.76200535G>A; NC_000001.10:g.76200535G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003774.2, RCV000211526.1,