Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 45
rs200928781
CHEK2
0.752 0.240 22 28695800 missense variant T/A;C;G snv 2.4E-05 10
rs137853011
CHEK2
0.763 0.280 22 28695219 missense variant G/A snv 4.9E-04 2.6E-04 6
rs200050883
CHEK2
0.851 0.120 22 28695190 missense variant C/A;G;T snv 3.9E-04 3.4E-04 4
rs536907995
CHEK2
0.882 0.120 22 28734664 stop gained G/A snv 1.4E-04 2.8E-05 4
rs587780170
CHEK2
0.851 0.120 22 28695786 missense variant C/A;G;T snv 2.8E-05; 8.0E-06 4
rs9620817
CHEK2
0.851 0.120 22 28712568 intron variant A/T snv 8.4E-02 4
rs28909982
CHEK2
0.925 0.080 22 28725338 missense variant T/C snv 1.2E-04 9.1E-05 3
rs531398630
CHEK2
0.882 0.160 22 28695858 missense variant G/A snv 4.8E-04 1.1E-04 3
rs72552322
CHEK2
0.925 0.120 22 28725070 missense variant C/T snv 2.4E-05 7.0E-06 3
rs1175088679
CHEK2
0.925 0.080 22 28695764 missense variant G/A snv 2
rs137853007
CHEK2
0.790 0.240 22 28725254 missense variant G/A;T snv 5.2E-05 2
rs137853010
CHEK2
0.882 0.120 22 28725028 missense variant G/A;C snv 1.1E-04 2
rs17883862
CHEK2
0.882 0.080 22 28734468 missense variant G/A;C;T snv 9.1E-04; 1.2E-05 2
rs200649225
CHEK2
0.925 0.080 22 28695752 missense variant C/T snv 2.8E-04 1.1E-04 2
rs201206424
CHEK2
0.925 0.080 22 28696960 missense variant G/A;C;T snv 5.2E-05 7.0E-06 2
rs587780192
CHEK2
0.925 0.080 22 28699929 missense variant C/G;T snv 4.4E-05; 4.0E-06 2
rs587782527
CHEK2
0.925 0.080 22 28695753 missense variant G/A;T snv 5.2E-05; 2.0E-05 2
rs730881687
CHEK2
1.000 0.080 22 28710060 splice acceptor variant C/A;T snv 1.2E-05; 1.6E-05 2
rs730881701
CHEK2
0.827 0.200 22 28725278 stop gained G/A;C snv 2.4E-05 7.0E-06 2
rs766794072
CHEK2
0.925 0.080 22 28699890 missense variant A/G snv 4.0E-06 2
rs77130927
CHEK2
0.882 0.120 22 28725031 missense variant G/A snv 1.0E-03 5.5E-04 2