rs4720169, TBX20

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.
Congenital Heart Defects
CUI: C0018798
Disease: Congenital Heart Defects
58 1.000 0.040 7 35247689 intron variant G/A snv 0.53 0.010 1.000 1 2019 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 1.000 0.040 7 35247689 intron variant G/A snv 0.53 0.010 1.000 1 2019 2019