Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs778561687
AKT2
0.851 0.080 19 40235953 missense variant C/A;T snv 4.0E-06; 4.0E-06 4
rs754845817
ALDH2
1.000 0.080 12 111790494 missense variant G/A snv 1.6E-05 1.4E-05 1
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv 14
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs1057519781
ALK
0.807 0.160 2 29209816 missense variant C/G snv 9
rs1057519698
ALK
0.827 0.120 2 29222347 missense variant A/G;T snv 8
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 7
rs113994088
ALK
0.925 0.080 2 29222584 missense variant C/G snv 4
rs113994091
ALK
0.882 0.160 2 29222407 missense variant G/A;C snv 3.2E-05 4
rs751306825
ALK
0.925 0.080 2 29220759 missense variant G/A;T snv 4.0E-06 4
rs863225283
ALK
0.925 0.080 2 29213993 missense variant A/C snv 4
rs550608288
ALK
1.000 0.080 2 29717646 missense variant T/C snv 5.2E-05 1
rs958335893
ALK
1.000 0.080 2 29193478 missense variant C/T snv 1
rs919968
ANKRD34C-AS1
1.000 0.080 15 79205004 intron variant T/A;G snv 1
rs41997
ANKRD7
1.000 0.080 7 118351841 intron variant A/G snv 0.27 1
rs369137693
ANTXR1
0.925 0.200 2 69193414 missense variant C/T snv 2.8E-05 1.4E-05 2
rs747908253
ANTXR1
0.925 0.200 2 69182599 missense variant G/A snv 1.6E-05 2
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs148298598
APEX1
0.925 0.200 14 20457111 missense variant G/A snv 2.3E-04 2.1E-04 2
rs2307486
APEX1 ; OSGEP
0.790 0.240 14 20456045 missense variant A/G snv 7.4E-03 2.1E-03 7
rs751661633
APOBEC3A ; APOBEC3B
0.851 0.120 22 38984136 missense variant C/A snv 4.1E-06 6
rs763375936
ATG3
0.827 0.160 3 112532749 missense variant C/T snv 8.3E-06 7.0E-06 5
rs772776695
ATG3
0.827 0.160 3 112548576 missense variant T/A snv 4.0E-06 5
rs2245214
ATG5
0.827 0.240 6 106214866 intron variant C/G snv 0.42 6
rs751688663
ATG7
0.807 0.280 3 11340656 missense variant G/A snv 4.0E-06 7