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rs777998984

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs777998984(-;-)
Make rs777998984(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position75734829
GeneACADM
is asnp
is mentioned by
dbSNPrs777998984
ebirs777998984
HLIrs777998984
Exacrs777998984
Varsomers777998984
Maprs777998984
PheGenIrs777998984
hapmaprs777998984
1000 genomesrs777998984
hgdprs777998984
ensemblrs777998984
gopubmedrs777998984
geneviewrs777998984
scholarrs777998984
googlers777998984
pharmgkbrs777998984
gwascentralrs777998984
openSNPrs777998984
23andMers777998984
23andMe allrs777998984
SNP Nexus

SNPshotrs777998984
SNPdbers777998984
MSV3drs777998984
GWAS Ctlgrs777998984
Max Magnitude0
ClinVar
Risk rs777998984(;)
Alt rs777998984(;)
Reference rs777998984(G;G)
Significance Pathogenic
Disease not provided Medium-chain acyl-coenzyme A dehydrogenase deficiency
Variation info
Gene ACADM
CLNDBN not provided Medium-chain acyl-coenzyme A dehydrogenase deficiency
Reversed 0
HGVS NC_000001.10:g.76200514delG
CLNSRC
CLNACC RCV000185675.1, RCV000211535.1,