rs77931234, ACADM

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Medium-chain acyl-coenzyme A dehydrogenase deficiency
114 0.925 0.120 1 75761161 missense variant A/C;G snv 3.3E-03 0.900 1.000 58 1990 2020
Sudden infant death syndrome
CUI: C0038644
Disease: Sudden infant death syndrome
68 0.925 0.120 1 75761161 missense variant A/C;G snv 3.3E-03 0.010 1.000 1 1996 1996
Vomiting
CUI: C0042963
Disease: Vomiting
23 0.925 0.120 1 75761161 missense variant A/C;G snv 3.3E-03 0.010 1.000 1 2010 2010