rs1343372308, MYH7;MHRT

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.
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 14 23413792 missense variant C/G snv 7.0E-06 0.010 1.000 1 2017 2017
Congenital Heart Defects
CUI: C0018798
Disease: Congenital Heart Defects
58 14 23413792 missense variant C/G snv 7.0E-06 0.010 1.000 1 2017 2017