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rs121434274

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434274(A;A)
Make rs121434274(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position75749509
GeneACADM
is asnp
is mentioned by
dbSNPrs121434274
ebirs121434274
HLIrs121434274
Exacrs121434274
Varsomers121434274
Maprs121434274
PheGenIrs121434274
hapmaprs121434274
1000 genomesrs121434274
hgdprs121434274
ensemblrs121434274
gopubmedrs121434274
geneviewrs121434274
scholarrs121434274
googlers121434274
pharmgkbrs121434274
gwascentralrs121434274
openSNPrs121434274
23andMers121434274
23andMe allrs121434274
SNP Nexus

SNPshotrs121434274
SNPdbers121434274
MSV3drs121434274
GWAS Ctlgrs121434274
Max Magnitude0
OMIM607008
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121434274(A;A)
Alt rs121434274(A;A)
Reference rs121434274(G;G)
Significance Pathogenic
Disease Medium-chain acyl-coenzyme A dehydrogenase deficiency not provided
Variation info
Gene ACADM
CLNDBN Medium-chain acyl-coenzyme A dehydrogenase deficiency not provided
Reversed 0
HGVS NC_000001.10:g.76215194G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003771.2, RCV000185665.2,