Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs766736182
IL7
0.925 0.080 8 78733724 missense variant T/C snv 4.2E-06 2
rs17505589
IL7
8 78777400 intron variant C/T snv 7.3E-02 1
rs2919917
IL7
8 78745028 intron variant T/C snv 0.34 1