Disease: Coronary heart disease
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs2523535 0.851 0.200 6 31368473 intron variant A/G snv 0.32 7
rs9268402
TSBP1 ; TSBP1-AS1
0.827 0.200 6 32373576 intron variant G/A snv 0.45 4