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rs1057518677

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518677(A;G)
Make rs1057518677(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position75733526
GeneACADM
is asnp
is mentioned by
dbSNPrs1057518677
dbSNP (classic)rs1057518677
ClinGenrs1057518677
ebirs1057518677
HLIrs1057518677
Exacrs1057518677
Gnomadrs1057518677
Varsomers1057518677
LitVarrs1057518677
Maprs1057518677
PheGenIrs1057518677
Biobankrs1057518677
1000 genomesrs1057518677
hgdprs1057518677
ensemblrs1057518677
geneviewrs1057518677
scholarrs1057518677
googlers1057518677
pharmgkbrs1057518677
gwascentralrs1057518677
openSNPrs1057518677
23andMers1057518677
23andMe allrs1057518677
SNPshotrs1057518677
SNPdbers1057518677
MSV3drs1057518677
GWAS Ctlgrs1057518677
Max Magnitude0
ClinVar
Risk rs1057518677(G;G)
Alt rs1057518677(G;G)
Reference Rs1057518677(A;A)
Significance 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.76199211A>G
CLNSRC
CLNACC RCV000415233.1,