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.
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
CUI: C4551768
Disease: CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
44 0.925 0.160 19 15180807 missense variant G/A snv 0.800 1.000 23 1997 2015
CADASIL Syndrome
CUI: C0751587
Disease: CADASIL Syndrome
23 0.925 0.160 19 15180807 missense variant G/A snv 0.020 1.000 2 2006 2009
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 0.925 0.160 19 15180807 missense variant G/A snv 0.010 1.000 1 2016 2016