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rs786204424

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204424(-;-)
Make rs786204424(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position75733629
GeneACADM
is asnp
is mentioned by
dbSNPrs786204424
ebirs786204424
HLIrs786204424
Exacrs786204424
Varsomers786204424
Maprs786204424
PheGenIrs786204424
hapmaprs786204424
1000 genomesrs786204424
hgdprs786204424
ensemblrs786204424
gopubmedrs786204424
geneviewrs786204424
scholarrs786204424
googlers786204424
pharmgkbrs786204424
gwascentralrs786204424
openSNPrs786204424
23andMers786204424
23andMe allrs786204424
SNP Nexus

SNPshotrs786204424
SNPdbers786204424
MSV3drs786204424
GWAS Ctlgrs786204424
Max Magnitude0
ClinVar
Risk rs786204424(;)
Alt rs786204424(;)
Reference rs786204424(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.76199314delG
CLNSRC Counsyl
CLNACC RCV000169015.1,