Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs530941076
TP53
0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 21
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs121913412
CTNNB1
0.724 0.280 3 41224633 missense variant A/C;G;T snv 19
rs864622237
TP53
0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs397517201
PIK3CA
0.732 0.240 3 179218307 missense variant A/C;G;T snv 16
rs587782289
TP53
0.752 0.240 17 7674257 missense variant A/C;G;T snv 15
rs1057520006
TP53
0.752 0.240 17 7673799 missense variant A/C;G;T snv 14
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs1057519978
TP53
0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs765848205
TP53
0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs35107139
BMP4
0.776 0.080 14 53952388 intron variant A/C;G;T snv 11
rs4768903
DIP2B
0.790 0.080 12 50651666 intron variant A/C;G;T snv 9
rs121918465
PTPN11
0.827 0.200 12 112450407 missense variant A/C;G;T snv 7
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1057519938
PIK3CA
0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs2250430
PLEKHG6
0.776 0.080 12 6312008 intron variant A/C;T snv 10
rs4450168
SBF2
0.790 0.080 11 10265208 intron variant A/C;T snv 0.12 9
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78