Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913273
PIK3CA
0.605 0.440 3 179218294 missense variant G/A;C snv 5
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 4
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 3
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 2
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 2
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 2
rs1429133479
MYO18B
1.000 0.080 22 25847461 missense variant G/A snv 1.4E-05 1
rs750078923
MYO18B
1.000 0.080 22 25769052 missense variant G/A;C snv 1.6E-05 1
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 1
rs121909229
PTEN
0.683 0.400 10 87933148 missense variant G/A;C;T snv 1
rs137853294
RB1
0.827 0.200 13 48459708 missense variant C/T snv 1.6E-05 1
rs1057519985
TP53
0.724 0.360 17 7673763 missense variant T/A;C;G snv 1
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 1
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 1
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 1
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 1
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 1
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 1
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 1
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 1
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 1
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 1
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 1
rs985033810
TP53
0.724 0.280 17 7674232 missense variant C/A;G;T snv 1