Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137852569
AR
0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 10
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 10
rs6152
AR
0.763 0.240 X 67545785 synonymous variant G/A snv 0.15 0.28 9
rs1057519864
AR
0.851 0.080 X 67723707 missense variant T/C snv 8
rs137852593
AR
0.827 0.160 X 67717484 missense variant G/A;C;T snv 2.2E-05; 1.1E-05; 9.1E-04 8
rs976306779
AR
0.851 0.080 X 67545492 missense variant C/A;T snv 6.6E-06 8
rs137852581
AR
0.882 0.080 X 67723701 missense variant C/T snv 5
rs864622007
AR
0.882 0.200 X 67711621 missense variant T/A snv 5
rs1034866440
AR
0.851 0.160 X 67643401 missense variant G/A snv 5.7E-06 4
rs137852571
AR
0.882 0.080 X 67717495 missense variant G/A snv 7.7E-05 1.9E-05 3
rs6624304
AR
0.882 0.160 X 67655914 intron variant T/A;C snv 3
rs968098233
AR
0.882 0.200 X 67546162 missense variant T/C snv 3
rs139756052
AR
0.925 0.080 X 67643314 missense variant A/T snv 1.3E-04 5.6E-04 2
rs777787518
AR
0.925 0.080 X 67545298 missense variant G/A snv 2