Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs377035972 14 24155679 missense variant G/A snv 5.6E-05 9.8E-05 1
rs756386867 X 38160977 missense variant C/G snv 1.1E-05 9.5E-06 1
rs1363884891 18 12673471 missense variant C/T snv 7.0E-06 1
rs121918457 0.701 0.280 12 112488466 missense variant C/T snv 4.0E-06 7.0E-06 18
rs1010184002 0.689 0.400 6 42978878 stop gained C/T snv 7.0E-06 60
rs1480591236 1 228276699 missense variant C/T snv 7.0E-06 1
rs759951698 14 23139485 missense variant T/C snv 8.0E-06 7.0E-06 1
rs28933386 0.752 0.400 12 112477719 missense variant A/G snv 1.2E-05 7.0E-06 14
rs121912855 0.851 0.200 3 48575218 missense variant G/A snv 2.0E-05 7.0E-06 15
rs747867083 1 19119624 missense variant C/T snv 4.0E-06 7.0E-06 1
rs1057519324 0.925 0.080 9 35801153 stop gained C/T snv 7.0E-06 4
rs1441510334 5 171436234 missense variant C/T snv 7.0E-06 1
rs267607048 0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 12
rs189150283 0.925 22 20992304 stop gained C/T snv 6.0E-05 7.0E-05 3
rs752482499 14 23140529 missense variant C/T snv 1.2E-05 7.0E-06 1
rs121918459 0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 46
rs201306926 4 140399004 missense variant T/C snv 3.6E-05 7.0E-06 1
rs368869806 0.614 0.480 9 95485875 splice acceptor variant C/T snv 4.0E-06 7.0E-06 97
rs1344172059 0.882 0.080 11 17430838 missense variant C/T snv 7.0E-06 12
rs760929207 0.925 0.200 2 219568050 splice donor variant ACCTTTGACTG/- delins 8.1E-06 7.0E-06 12
rs763505389 17 78491549 missense variant C/T snv 1.6E-05 7.0E-06 1
rs121912854 0.851 0.200 3 48592915 stop gained G/A snv 1.2E-05 7.0E-06 16
rs747762087 3 73384465 missense variant T/A;G snv 7.0E-06 1
rs752298579 0.701 0.480 22 20061538 missense variant G/A snv 1.4E-04 7.0E-06 48
rs397509426 0.882 0.080 3 49723632 missense variant G/A snv 8.0E-05 7.0E-06 7