Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 7
rs121913273
PIK3CA
0.605 0.440 3 179218294 missense variant G/A;C snv 5
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 4
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 4
rs55770810
BRCA1
0.763 0.280 17 43063931 missense variant G/A;T snv 2.4E-05; 8.0E-06 3
rs80357474
BRCA1
0.827 0.200 17 43049188 missense variant A/C;G;T snv 8.0E-06 3
rs61753793
FBXO11 ; MSH6
0.851 0.120 2 47799002 missense variant T/C snv 3.6E-05 5.6E-05 3
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 3
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 3
rs4148323
UGT1A10 ; UGT1A9 ; UGT1A7 ; UGT1A3 ; UGT1A5 ; UGT1A6 ; UGT1A8 ; UGT1A1 ; UGT1A4
0.701 0.440 2 233760498 missense variant G/A snv 2.2E-02 9.2E-03 3
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 2
rs397514606
AKT3
0.763 0.320 1 243695714 missense variant C/T snv 2
rs137852573
AR
0.807 0.280 X 67686064 missense variant G/A snv 2
rs137852576
AR
0.827 0.240 X 67686067 missense variant G/A snv 2
rs273900729
BRCA1
0.925 0.160 17 43082529 missense variant A/G snv 2
rs28897672
BRCA1
0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 2
rs45553935
BRCA1
0.851 0.200 17 43057122 missense variant A/C;G;T snv 2
rs56214134
BRCA1
0.925 0.080 17 43091931 missense variant C/A;G snv 1.2E-04; 2.3E-04 2
rs41293521
BRCA2
0.925 0.160 13 32394724 missense variant T/C snv 2.9E-04 2.5E-04 2
rs4987046
BRCA2
0.925 0.160 13 32319134 missense variant A/G snv 1.6E-03 1.6E-03 2
rs80358451
BRCA2
0.925 0.160 13 32333140 missense variant T/G snv 5.6E-05 6.3E-05 2
rs80359078
BRCA2
0.882 0.160 13 32370430 missense variant G/A snv 3.2E-05 2.1E-05 2
rs137853007
CHEK2
0.790 0.240 22 28725254 missense variant G/A;T snv 5.2E-05 2
rs61732504
HLCS
0.925 0.160 21 36937319 missense variant C/A;T snv 2.2E-02; 4.0E-06 2
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 2