rs397516373, TPM1

N. diseases: 4
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 0.925 0.080 15 63059663 missense variant G/A snv 0.700 1.000 5 2016 2018
Cardiomyopathy, Hypertrophic, Familial
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
355 0.925 0.080 15 63059663 missense variant G/A snv 0.700 1.000 3 2011 2017
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.925 0.080 15 63059663 missense variant G/A snv 0.700 0
LEFT VENTRICULAR NONCOMPACTION 9
CUI: C3808145
Disease: LEFT VENTRICULAR NONCOMPACTION 9
4 0.925 0.080 15 63059663 missense variant G/A snv 0.700 0