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rs1057517179

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs1057517179(-;-)
Make rs1057517179(-;AG)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position75732698
GeneACADM
is asnp
is mentioned by
dbSNPrs1057517179
dbSNP (old)rs1057517179
ClinGenrs1057517179
ebirs1057517179
HLIrs1057517179
Exacrs1057517179
Gnomadrs1057517179
Varsomers1057517179
Maprs1057517179
PheGenIrs1057517179
Biobankrs1057517179
1000 genomesrs1057517179
hgdprs1057517179
ensemblrs1057517179
gopubmedrs1057517179
geneviewrs1057517179
scholarrs1057517179
googlers1057517179
pharmgkbrs1057517179
gwascentralrs1057517179
openSNPrs1057517179
23andMers1057517179
23andMe allrs1057517179
SNPshotrs1057517179
SNPdbers1057517179
MSV3drs1057517179
GWAS Ctlgrs1057517179
Max Magnitude0
ClinVar
Risk rs1057517179(-;-)
Alt rs1057517179(-;-)
Reference Rs1057517179(AG;AG)
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.76198383_76198384delAG
CLNSRC
CLNACC RCV000410859.1,