Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs4646903
CYP1A1
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs121909231
PTEN
0.667 0.600 10 87961095 stop gained C/A;T snv 32
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs28934574
TP53
0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 31
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 28
rs121912656
TP53
0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 28
rs28934573
TP53
0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 28
rs121913400
CTNNB1
0.683 0.360 3 41224610 missense variant C/A;G;T snv 26
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs121913275
PIK3CA
0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 26
rs1057519991
TP53
0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 26
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs1057519925
PIK3CA
0.683 0.560 3 179210291 missense variant G/A;C snv 25
rs138729528
TP53
0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 24
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24