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.
Cardiomyopathy, Hypertrophic, Familial
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
355 0.925 0.200 MT 4295 non coding transcript exon variant A/G snv 0.700 0
DEAFNESS, NONSYNDROMIC SENSORINEURAL, MITOCHONDRIAL
CUI: C3151897
Disease: DEAFNESS, NONSYNDROMIC SENSORINEURAL, MITOCHONDRIAL
8 0.925 0.200 MT 4295 non coding transcript exon variant A/G snv 0.700 0