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rs121434278

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434278(A;A)
Make rs121434278(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position75740094
GeneACADM
is asnp
is mentioned by
dbSNPrs121434278
ebirs121434278
HLIrs121434278
Exacrs121434278
Varsomers121434278
Maprs121434278
PheGenIrs121434278
hapmaprs121434278
1000 genomesrs121434278
hgdprs121434278
ensemblrs121434278
gopubmedrs121434278
geneviewrs121434278
scholarrs121434278
googlers121434278
pharmgkbrs121434278
gwascentralrs121434278
openSNPrs121434278
23andMers121434278
23andMe allrs121434278
SNP Nexus

SNPshotrs121434278
SNPdbers121434278
MSV3drs121434278
GWAS Ctlgrs121434278
Max Magnitude0
OMIM607008
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121434278(A;A)
Alt rs121434278(A;A)
Reference rs121434278(G;G)
Significance Other
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.76205779G>A
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000003777.5, RCV000077891.3,