Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2279115
BCL2
0.724 0.320 18 63319604 5 prime UTR variant G/A;T snv 18
rs1800477
BCL2
0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 12
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 9
rs17757541
BCL2
0.827 0.240 18 63212453 intron variant C/G;T snv 7
rs1801018
BCL2
0.851 0.240 18 63318646 synonymous variant T/C snv 0.37 0.32 6
rs780634396
BCL2
0.882 0.120 18 63318618 missense variant T/C snv 4.0E-06 5
rs1564483
BCL2
1.000 0.080 18 63127421 3 prime UTR variant C/T snv 0.22 4
rs17759659
BCL2
0.851 0.120 18 63291411 intron variant A/G snv 0.31 4
rs3744935
BCL2
0.882 0.080 18 63127447 3 prime UTR variant C/T snv 6.0E-03 3
rs4987852
BCL2
0.925 0.120 18 63126688 3 prime UTR variant T/C snv 5.1E-02 3
rs4987867
BCL2
18 63123839 3 prime UTR variant C/T snv 6.4E-03 3
rs7226979
BCL2
0.925 0.120 18 63257737 intron variant C/T snv 0.42 3
rs747504890
BCL2
0.925 0.080 18 63318285 missense variant C/T snv 2.4E-05 3
rs1473418
BCL2
1.000 0.080 18 63319316 5 prime UTR variant C/G snv 0.98 2
rs4940576
BCL2
0.925 0.040 18 63181406 intron variant T/A;C snv 2
rs4987855
BCL2
0.925 0.120 18 63126316 3 prime UTR variant C/T snv 5.9E-02 2
rs4987856
BCL2
0.925 0.120 18 63126261 3 prime UTR variant C/T snv 6.0E-02 2
rs12457893
BCL2
1.000 0.080 18 63258928 intron variant A/C snv 0.39 1
rs1310296388
BCL2
1.000 0.080 18 63318110 missense variant T/C snv 4.0E-06 1
rs187971642
BCL2
18 63213468 intron variant T/C snv 4.1E-03 1
rs4987853
BCL2
1.000 0.120 18 63126422 3 prime UTR variant T/C;G snv 0.23 1
rs533722308
BCL2
1.000 0.080 18 63293961 intron variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTTTT delins 1
rs720321
BCL2
1.000 0.080 18 63215417 intron variant G/A snv 0.21 1