rs140523053, TRIM63

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.
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 1.000 0.040 1 26067352 missense variant G/A snv 1.4E-03 1.3E-03 0.010 1.000 1 2012 2012