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

rs747268471

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common genotype
Make rs747268471(A;A)
Make rs747268471(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position75750529
GeneACADM
is asnp
is mentioned by
dbSNPrs747268471
dbSNP (classic)rs747268471
ClinGenrs747268471
ebirs747268471
HLIrs747268471
Exacrs747268471
Gnomadrs747268471
Varsomers747268471
LitVarrs747268471
Maprs747268471
PheGenIrs747268471
Biobankrs747268471
1000 genomesrs747268471
hgdprs747268471
ensemblrs747268471
geneviewrs747268471
scholarrs747268471
googlers747268471
pharmgkbrs747268471
gwascentralrs747268471
openSNPrs747268471
23andMers747268471
SNPshotrs747268471
SNPdbers747268471
MSV3drs747268471
GWAS Ctlgrs747268471
Max Magnitude0
ClinVar
Risk rs747268471(A;A)
Alt rs747268471(A;A)
Reference Rs747268471(G;G)
Significance Other
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.76216214G>A
CLNSRC
CLNACC RCV000173613.1,