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rs1057516278

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057516278(-;G)
Make rs1057516278(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position75761290
GeneACADM
is asnp
is mentioned by
dbSNPrs1057516278
dbSNP (old)rs1057516278
ClinGenrs1057516278
ebirs1057516278
HLIrs1057516278
Exacrs1057516278
Gnomadrs1057516278
Varsomers1057516278
Maprs1057516278
PheGenIrs1057516278
Biobankrs1057516278
1000 genomesrs1057516278
hgdprs1057516278
ensemblrs1057516278
gopubmedrs1057516278
geneviewrs1057516278
scholarrs1057516278
googlers1057516278
pharmgkbrs1057516278
gwascentralrs1057516278
openSNPrs1057516278
23andMers1057516278
23andMe allrs1057516278
SNPshotrs1057516278
SNPdbers1057516278
MSV3drs1057516278
GWAS Ctlgrs1057516278
Max Magnitude0
ClinVar
Risk rs1057516278(G;G)
Alt rs1057516278(G;G)
Reference Rs1057516278(-;-)
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.76226975dupG
CLNSRC
CLNACC RCV000410007.1,