Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1034265990
CDKN2A
0.925 0.120 9 21971123 missense variant G/A;T snv 4.4E-06 2
rs104894094
CDKN2A
0.763 0.200 9 21971058 missense variant C/A;G;T snv 8.5E-06; 4.3E-06 12
rs104894095
CDKN2A
0.827 0.120 9 21971200 missense variant C/G;T snv 9.0E-06 6
rs104894097
CDKN2A
0.807 0.240 9 21974757 missense variant C/A;G;T snv 1.7E-05; 1.3E-05 8
rs104894098
CDKN2A
0.851 0.200 9 21970982 missense variant A/T snv 5
rs104894099
CDKN2A
0.851 0.200 9 21971183 missense variant A/C;T snv 4.6E-06 5
rs104894104
CDKN2A
0.790 0.160 9 21971019 missense variant G/A;T snv 7
rs104894109
CDKN2A
0.925 0.120 9 21971192 missense variant C/A;T snv 3
rs1057519852
CDKN2A
9 21971030 stop gained C/T snv 1
rs1057519881
CDKN2A
0.776 0.240 9 21971111 missense variant T/C snv 8
rs1057519882
CDKN2A
0.807 0.200 9 21974678 missense variant C/A snv 7
rs1057519883
CDKN2A
0.742 0.280 9 21971120 missense variant C/G;T snv 14
rs1060501260
CDKN2A
9 21971156 missense variant G/A;C snv 4.7E-06 1
rs1060501262
CDKN2A ; CDKN2B-AS1
1.000 0.120 9 21994138 splice donor variant C/T snv 1
rs1060501263
CDKN2A
1.000 0.120 9 21971001 frameshift variant C/- delins 2
rs1060501265
CDKN2A
1.000 0.120 9 21974676 splice donor variant A/G snv 1
rs1060501266
CDKN2A
1.000 0.120 9 21968347 intron variant T/C snv 7.0E-06 1
rs1060504185
CDKN2A
9 21971116 missense variant G/A;C snv 1
rs1064794292
CDKN2A
0.882 0.200 9 21974760 missense variant C/T snv 3
rs1131691186
CDKN2A
0.925 0.120 9 21974761 missense variant C/A;T snv 3
rs1131691187
CDKN2A
1.000 0.120 9 21974696 frameshift variant G/- del 2
rs1131691188
CDKN2A
9 21974782 frameshift variant -/C delins 1
rs113798404
CDKN2A
0.925 0.080 9 21970995 missense variant C/G;T snv 2
rs11515
CDKN2A ; CDKN2A-DT
0.882 0.040 9 21968200 3 prime UTR variant C/A;G snv 4.0E-06; 0.88 6
rs11552822
CDKN2A
1.000 9 21971109 missense variant C/A;T snv 4.3E-06 2