Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6871536
RAD50 ; TH2LCRR
0.827 0.160 5 132634182 intron variant T/C snv 0.24 2
rs17772583
RAD50
0.925 0.120 5 132617818 intron variant A/G snv 0.18 1
rs2244012
RAD50
1.000 0.080 5 132565533 intron variant A/G snv 0.33 1
rs2240032
TH2LCRR ; RAD50
1.000 0.080 5 132641435 intron variant C/G;T snv 1