rs104893749, MYL3

N. diseases: 2
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, FAMILIAL HYPERTROPHIC, 8
CUI: C1837471
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8
8 0.925 0.080 3 46859495 missense variant C/A;T snv 4.0E-06; 2.4E-05 0.800 1.000 4 1996 2013
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
CUI: C3495498
Disease: Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
163 0.925 0.080 3 46859495 missense variant C/A;T snv 4.0E-06; 2.4E-05 0.700 1.000 2 1996 2012