rs367785431, TNNT2

N. diseases: 1
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, 2
CUI: C1861864
Disease: Cardiomyopathy, Familial Hypertrophic, 2
30 1.000 0.080 1 201359221 missense variant G/A;T snv 2.5E-05 7.0E-06 0.700 1.000 14 1994 2012