Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1860661
TCF3
0.882 0.120 19 1650135 intron variant A/C;G snv 6.7E-06; 0.54 3
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53