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rs768884003

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs768884003(A;A)
Make rs768884003(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position75749467
GeneACADM
is asnp
is mentioned by
dbSNPrs768884003
ebirs768884003
HLIrs768884003
Exacrs768884003
Varsomers768884003
Maprs768884003
PheGenIrs768884003
hapmaprs768884003
1000 genomesrs768884003
hgdprs768884003
ensemblrs768884003
gopubmedrs768884003
geneviewrs768884003
scholarrs768884003
googlers768884003
pharmgkbrs768884003
gwascentralrs768884003
openSNPrs768884003
23andMers768884003
23andMe allrs768884003
SNP Nexus

SNPshotrs768884003
SNPdbers768884003
MSV3drs768884003
GWAS Ctlgrs768884003
Max Magnitude0
ClinVar
Risk rs768884003(A;A)
Alt rs768884003(A;A)
Reference rs768884003(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.76215152G>A
CLNSRC
CLNACC RCV000211500.1,