Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs13347 0.763 0.320 11 35231725 3 prime UTR variant C/A;T snv 12
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs7164773 0.790 0.240 15 60775749 intron variant C/A;T snv 10
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs12529 0.776 0.280 10 5094459 missense variant C/G snv 0.50 0.45 10
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2227310 0.807 0.160 10 113729393 missense variant C/G snv 0.26 0.23 9
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3660 0.882 0.160 12 52286153 3 prime UTR variant C/G snv 0.51 6
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs941759532 0.763 0.240 16 13932175 missense variant C/G snv 11
rs16917496 0.689 0.360 12 123409283 3 prime UTR variant C/G;T snv 21
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs3740066 0.724 0.440 10 99844450 missense variant C/G;T snv 2.4E-05; 0.34 20
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs745564626 0.752 0.280 14 103699003 missense variant C/G;T snv 4.3E-05 14