Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
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
rs864622237
TP53
0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs1057520006
TP53
0.752 0.240 17 7673799 missense variant A/C;G;T snv 14
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs876658657
MLH1
0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs4760
PLAUR
1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11 8
rs859
STARD5 ; IL16
0.807 0.200 15 81308981 3 prime UTR variant A/G snv 0.33 6
rs6790167
TP63
0.827 0.080 3 189869485 intron variant A/G snv 0.53 5
rs141877527 1.000 0.080 10 33497992 intergenic variant A/G snv 7.3E-03 1
rs716274 1.000 0.080 11 103547430 intergenic variant A/G snv 0.51 1
rs8049634
LOC654780 ; ADAD2
1.000 0.080 16 84192073 intron variant A/G snv 0.35 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs121913682
KIT
0.605 0.400 4 54733167 missense variant A/G;T snv 52
rs1023835002
B2M ; PATL2
0.763 0.280 15 44711547 start lost A/G;T snv 10
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 49
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs141670911 1.000 0.080 6 26581030 intergenic variant A/T snv 7.3E-02 1
rs1899663
HOTAIR
0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs1057520005
TP53
0.742 0.360 17 7673800 missense variant C/A;G snv 14