Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913281
PIK3CA
0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 30
rs121909231
PTEN
0.667 0.600 10 87961095 stop gained C/A;T snv 29
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs121913273
PIK3CA
0.605 0.440 3 179218294 missense variant G/A;C snv 25
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 25
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 25
rs1057519925
PIK3CA
0.683 0.560 3 179210291 missense variant G/A;C snv 24
rs121909219
PTEN
0.689 0.400 10 87957915 stop gained C/A;T snv 24
rs121909229
PTEN
0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 22
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 21
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs1057520002
TP53
0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 19
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 19
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 19
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 19
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 18
rs4808075
BABAM1 ; USHBP1
0.701 0.280 19 17279482 intron variant T/C snv 0.26 18
rs56084662
FRY
0.701 0.280 13 32295727 3 prime UTR variant G/A snv 3.5E-03 18
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 18