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rs1057516644

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516644(A;A)
Make rs1057516644(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position75749418
GeneACADM
is asnp
is mentioned by
dbSNPrs1057516644
dbSNP (classic)rs1057516644
ClinGenrs1057516644
ebirs1057516644
HLIrs1057516644
Exacrs1057516644
Gnomadrs1057516644
Varsomers1057516644
LitVarrs1057516644
Maprs1057516644
PheGenIrs1057516644
Biobankrs1057516644
1000 genomesrs1057516644
hgdprs1057516644
ensemblrs1057516644
geneviewrs1057516644
scholarrs1057516644
googlers1057516644
pharmgkbrs1057516644
gwascentralrs1057516644
openSNPrs1057516644
23andMers1057516644
SNPshotrs1057516644
SNPdbers1057516644
MSV3drs1057516644
GWAS Ctlgrs1057516644
Max Magnitude0
ClinVar
Risk rs1057516644(A;A)
Alt rs1057516644(A;A)
Reference Rs1057516644(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.76215103G>A
CLNSRC
CLNACC RCV000410883.1,