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rs147559466

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs147559466(A;A)
Make rs147559466(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position75732652
GeneACADM
is asnp
is mentioned by
dbSNPrs147559466
ebirs147559466
HLIrs147559466
Exacrs147559466
Varsomers147559466
Maprs147559466
PheGenIrs147559466
hapmaprs147559466
1000 genomesrs147559466
hgdprs147559466
ensemblrs147559466
gopubmedrs147559466
geneviewrs147559466
scholarrs147559466
googlers147559466
pharmgkbrs147559466
gwascentralrs147559466
openSNPrs147559466
23andMers147559466
23andMe allrs147559466
SNP Nexus

SNPshotrs147559466
SNPdbers147559466
MSV3drs147559466
GWAS Ctlgrs147559466
Max Magnitude0
ClinVar
Risk rs147559466(A;A)
Alt rs147559466(A;A)
Reference rs147559466(G;G)
Significance Other
Disease not provided Medium-chain acyl-coenzyme A dehydrogenase deficiency not specified
Variation info
Gene ACADM
CLNDBN not provided Medium-chain acyl-coenzyme A dehydrogenase deficiency not specified
Reversed 0
HGVS NC_000001.10:g.76198337G>A
CLNSRC HGMD
CLNACC RCV000077881.7, RCV000176959.1, RCV000185638.1,