Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs121913273
PIK3CA
0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs4919510
SEMA4G ; MIR608 ; MRPL43
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs28934571
TP53
0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs2227982
LOC105373977 ; PDCD1
0.677 0.480 2 241851281 missense variant G/A snv 9.2E-02 4.3E-02 24
rs1130214
AKT1
0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs749539903
ERBB2 ; MIR4728
0.827 0.120 17 39726987 missense variant G/A snv 8.4E-06 9
rs2946834
LINC02456 ; HELLPAR
0.807 0.200 12 102394036 non coding transcript exon variant A/G snv 0.63 7
rs759478535
ERBB2
0.851 0.080 17 39708351 missense variant A/G snv 6.8E-05 4.2E-05 6
rs28933368
ERBB2 ; MIR4728
0.851 0.080 17 39725721 missense variant G/A snv 5
rs10825036 0.882 0.080 10 53506471 intergenic variant T/G snv 0.21 3
rs166870 0.882 0.080 15 79777420 intergenic variant T/C;G snv 3
rs2071002
NQO2-AS1 ; NQO2
0.882 0.080 6 3000069 5 prime UTR variant A/C snv 0.32 3
rs387907158
PTPN11
0.882 0.160 12 112450475 stop gained A/T snv 3
rs2293554
CASP8
0.925 0.080 2 201266864 intron variant T/G snv 0.18 2
rs1484791833
ERBB4
0.925 0.080 2 211713624 missense variant G/A snv 2
rs1442481831
PIK3CA
0.925 0.080 3 179203635 missense variant T/C snv 2
rs186919241
PTPN11
0.925 0.080 12 112502165 missense variant G/A snv 4.0E-06 2