rs759589565, TXNRD1

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.
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.925 0.040 12 104321227 missense variant A/G snv 4.0E-05 3.5E-05 0.010 1.000 1 2014 2014
Hypertrophic obstructive cardiomyopathy
90 0.925 0.040 12 104321227 missense variant A/G snv 4.0E-05 3.5E-05 0.010 1.000 1 2014 2014