Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555429629
RAD51
0.763 0.200 15 40729632 missense variant G/A snv 23
rs1131692232
PUF60
0.851 0.160 8 143818426 inframe deletion GGGCAAAGG/- delins 6
rs1372410554
GLI1
1.000 0.080 12 57471334 missense variant A/G snv 3.5E-05 1