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rs875989869

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs875989869(A;A)
Make rs875989869(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position75739979
GeneACADM
is asnp
is mentioned by
dbSNPrs875989869
ebirs875989869
HLIrs875989869
Exacrs875989869
Varsomers875989869
Maprs875989869
PheGenIrs875989869
hapmaprs875989869
1000 genomesrs875989869
hgdprs875989869
ensemblrs875989869
gopubmedrs875989869
geneviewrs875989869
scholarrs875989869
googlers875989869
pharmgkbrs875989869
gwascentralrs875989869
openSNPrs875989869
23andMers875989869
23andMe allrs875989869
SNP Nexus

SNPshotrs875989869
SNPdbers875989869
MSV3drs875989869
GWAS Ctlgrs875989869
Max Magnitude0
ClinVar
Risk rs875989869(A;A)
Alt rs875989869(A;A)
Reference rs875989869(G;G)
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.76205664G>A
CLNSRC
CLNACC RCV000211431.1,