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

rs866388216

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs866388216(A;A)
Make rs866388216(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position75740111
GeneACADM
is asnp
is mentioned by
dbSNPrs866388216
ebirs866388216
HLIrs866388216
Exacrs866388216
Varsomers866388216
Maprs866388216
PheGenIrs866388216
hapmaprs866388216
1000 genomesrs866388216
hgdprs866388216
ensemblrs866388216
gopubmedrs866388216
geneviewrs866388216
scholarrs866388216
googlers866388216
pharmgkbrs866388216
gwascentralrs866388216
openSNPrs866388216
23andMers866388216
23andMe allrs866388216
SNP Nexus

SNPshotrs866388216
SNPdbers866388216
MSV3drs866388216
GWAS Ctlgrs866388216
Max Magnitude0
ClinVar
Risk rs866388216(A;A)
Alt rs866388216(A;A)
Reference rs866388216(G;G)
Significance Probable-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.76205796G>A
CLNSRC
CLNACC RCV000211443.1,