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rs875989874

From SNPedia

Geno Mag Summary
(;) 0 common in clinvar
is asnp
is mentioned by
dbSNPrs875989874
ebirs875989874
HLIrs875989874
Exacrs875989874
Varsomers875989874
Maprs875989874
PheGenIrs875989874
hapmaprs875989874
1000 genomesrs875989874
hgdprs875989874
ensemblrs875989874
gopubmedrs875989874
geneviewrs875989874
scholarrs875989874
googlers875989874
pharmgkbrs875989874
gwascentralrs875989874
openSNPrs875989874
23andMers875989874
23andMe allrs875989874
SNP Nexus

SNPshotrs875989874
SNPdbers875989874
MSV3drs875989874
GWAS Ctlgrs875989874
Max Magnitude0
ClinVar
Risk rs875989874(CTAGAATGAGTTA;CTAGAATGAGTTA)
Alt rs875989874(CTAGAATGAGTTA;CTAGAATGAGTTA)
Reference rs875989874(;)
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.76226873_76226874insTAGAATGAGTTAC
CLNSRC
CLNACC RCV000211550.1,