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rs875989875

From SNPedia

Geno Mag Summary
(;) 0 common in clinvar
is asnp
is mentioned by
dbSNPrs875989875
ebirs875989875
HLIrs875989875
Exacrs875989875
Varsomers875989875
Maprs875989875
PheGenIrs875989875
hapmaprs875989875
1000 genomesrs875989875
hgdprs875989875
ensemblrs875989875
gopubmedrs875989875
geneviewrs875989875
scholarrs875989875
googlers875989875
pharmgkbrs875989875
gwascentralrs875989875
openSNPrs875989875
23andMers875989875
23andMe allrs875989875
SNP Nexus

SNPshotrs875989875
SNPdbers875989875
MSV3drs875989875
GWAS Ctlgrs875989875
Max Magnitude0
ClinVar
Risk rs875989875(TTAGGAT;TTAGGAT)
Alt rs875989875(TTAGGAT;TTAGGAT)
Reference rs875989875(;)
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.76194162_76194168dupGATTTAG
CLNSRC
CLNACC RCV000211527.1,