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rs875989877

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs875989877(-;-)
Make rs875989877(-;T)
Make rs875989877(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position75761365
GeneACADM
is asnp
is mentioned by
dbSNPrs875989877
ebirs875989877
HLIrs875989877
Exacrs875989877
Varsomers875989877
Maprs875989877
PheGenIrs875989877
hapmaprs875989877
1000 genomesrs875989877
hgdprs875989877
ensemblrs875989877
gopubmedrs875989877
geneviewrs875989877
scholarrs875989877
googlers875989877
pharmgkbrs875989877
gwascentralrs875989877
openSNPrs875989877
23andMers875989877
23andMe allrs875989877
SNP Nexus

SNPshotrs875989877
SNPdbers875989877
MSV3drs875989877
GWAS Ctlgrs875989877
Max Magnitude0
ClinVar
Risk rs875989877(T;T)
Alt rs875989877(T;T)
Reference rs875989877(;)
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.76227050dupT
CLNSRC
CLNACC RCV000211490.1,