Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs370004591
TTN-AS1 ; TTN ; LOC101927055
1.000 0.080 2 178776789 missense variant C/T snv 4.0E-06 7.0E-06 1
rs374711533
DCLK3
1.000 0.080 3 36718103 missense variant G/A snv 9.2E-05 1.6E-04 1
rs770167074
BMP2K
1.000 0.080 4 78826060 missense variant G/A;C snv 1.6E-05; 4.0E-06 1
rs121913386
CDKN2A
0.807 0.120 9 21971018 missense variant G/A;T snv 1
rs121918499
FGFR2
0.925 0.160 10 121520048 missense variant C/A;G snv 1
rs772110575
PIK3CA
0.807 0.160 3 179198938 missense variant G/A;T snv 4.0E-06 1
rs1057519922
NFE2L2
0.790 0.200 2 177234082 missense variant C/G;T snv 1
rs121918465
PTPN11
0.827 0.200 12 112450407 missense variant A/C;G;T snv 1
rs121913351
BRAF
0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 2
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 1
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 1
rs1057519883
CDKN2A
0.742 0.280 9 21971120 missense variant C/G;T snv 1
rs587777790
PIK3CA
0.732 0.280 3 179199690 missense variant G/A snv 1
rs985033810
TP53
0.724 0.280 17 7674232 missense variant C/A;G;T snv 1
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 3
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 1
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 1
rs587782664
TP53
0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 1
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 2
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 1
rs397507546
PTPN11
0.790 0.360 12 112489084 missense variant G/A;C;T snv 1
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 1
rs867262025
PIK3CA
0.790 0.360 3 179221146 missense variant G/A snv 1
rs121913272
PIK3CA
0.752 0.400 3 179210192 missense variant T/C;G snv 3
rs121909229
PTEN
0.683 0.400 10 87933148 missense variant G/A;C;T snv 1