rs199476316, TPM1

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.
Cardiomyopathy, Hypertrophic, Familial
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
355 0.925 0.080 15 63062219 missense variant C/T snv 4.0E-06 7.0E-06 0.700 1.000 6 2008 2016
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.925 0.080 15 63062219 missense variant C/T snv 4.0E-06 7.0E-06 0.700 0
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.925 0.080 15 63062219 missense variant C/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2015 2015