Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs759435862
KIDINS220
0.925 0.080 2 8776852 missense variant C/A;T snv 2.0E-05 5
rs768949233
IAH1 ; ADAM17
0.851 0.040 2 9490466 missense variant G/C;T snv 4.0E-06 5
rs13423759
ERBB4
0.925 0.080 2 211381247 3 prime UTR variant A/C snv 6.8E-02 3
rs7371084
GTF2A1L ; LHCGR ; STON1-GTF2A1L
0.925 0.120 2 48712814 intron variant T/C snv 0.12 3
rs1156560901
CDK15
2 201880120 missense variant A/G snv 1.4E-05 2
rs992157
TMBIM1 ; PNKD
0.790 0.080 2 218290058 5 prime UTR variant G/A snv 0.46 2
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 66
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 62
rs3732379
CX3CR1
0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs1800734
EPM2AIP1 ; MLH1
0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs752021744
PIK3CB
0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 10
rs115160714
TOPBP1
0.807 0.200 3 133601021 3 prime UTR variant G/A snv 5.8E-03 9
rs373572
RAD18
0.882 0.120 3 8913705 missense variant C/T snv 0.68 0.70 6
rs7646409
PIK3CA
0.882 0.040 3 179182405 intron variant T/C snv 0.26 4
rs3731499
CDC25A
0.925 0.080 3 48184680 missense variant G/A snv 5.7E-05 1.2E-04 3
rs2118593
RYBP
1.000 0.080 3 72447740 upstream gene variant G/A;C;T snv 2
rs3206652
CD47
3 108046402 3 prime UTR variant T/C snv 0.27 1
rs3804639
CD47
3 108071988 intron variant G/T snv 0.28 1
rs71310379
PIK3CA
3 179199003 missense variant C/A snv 4.4E-05 4.2E-05 1
rs756160717
RAF1
3 12585204 missense variant G/A snv 1.2E-05 2.1E-05 1
rs9879947
CD47
3 108046545 3 prime UTR variant G/A snv 0.45 1
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 36
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs1057519710
KIT
0.695 0.280 4 54733166 missense variant G/C;T snv 22