Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519944
POLE
0.882 0.160 12 132676599 missense variant G/A snv 5
rs752742313
PIK3CB
0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 20
rs904571820
ESR1
0.851 0.160 6 151842664 start lost A/G snv 4.0E-06 5
rs796065354
ESR1
0.882 0.080 6 151944320 missense variant A/G snv 9
rs1462893414
ESR1
0.882 0.080 6 151944323 missense variant A/G snv 4.0E-06 7.0E-06 5
rs1057519827
ESR1
6 152011697 missense variant G/C snv 2
rs1057519714
ESR1
6 152094402 missense variant T/C snv 1
rs1057519715
ESR1
1.000 0.080 6 152098779 missense variant T/A snv 2
rs1057519716
ESR1
6 152098782 missense variant C/A snv 1
rs1057519717
ESR1
6 152098785 missense variant T/G snv 1
rs866987936
FBXW7
0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs747241612
FBXW7
0.752 0.240 4 152326215 missense variant G/C snv 4.0E-06 12
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 17
rs867384286
FBXW7
0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs753535070
MUC1
0.851 0.120 1 155187350 missense variant T/C snv 8.0E-06 5
rs1704754
HSD17B7
1 162790761 5 prime UTR variant C/T snv 0.70 0.62 1
rs555016384
CCR6
6 167136139 missense variant G/A snv 4.0E-06 7.0E-06 1
rs1057520036
FGFR4
0.925 0.080 5 177093180 missense variant A/G snv 3
rs1057519929
PIK3CA
0.776 0.320 3 179199066 missense variant G/A snv 10
rs121913287
PIK3CA
0.752 0.400 3 179199088 missense variant G/A snv 12
rs1057519933
PIK3CA
0.790 0.240 3 179199156 missense variant A/G snv 11
rs1057519935
PIK3CA
0.790 0.240 3 179199157 missense variant A/G snv 11
rs1057519934
PIK3CA
0.790 0.240 3 179199158 missense variant G/C snv 11
rs587777790
PIK3CA
0.732 0.280 3 179199690 missense variant G/A snv 14