Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11030104 0.790 0.240 11 27662970 intron variant A/G snv 0.16 8
rs11127292 0.925 0.160 2 2026171 intron variant C/T snv 0.11 2
rs12273539 0.925 0.120 11 27661764 intron variant C/T snv 0.12 2
rs3771863 0.925 0.240 2 75192588 intron variant C/T snv 0.30 2
rs2097903 1.000 0.080 7 10642782 intron variant A/T snv 0.51 1
rs35699176 1.000 0.080 19 2936537 stop gained G/A snv 3.1E-02 3.4E-02 1
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 264
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs2297518 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 29
rs1043210477 0.701 0.520 3 49358250 missense variant G/A snv 19
rs5522 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs224222 0.724 0.440 16 3254463 missense variant C/T snv 0.24 0.21 15
rs1129844 0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05 13
rs75634836 0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06 11
rs1314305899 0.807 0.280 7 151003224 missense variant C/T snv 7.9E-06 2.1E-05 6
rs1048101 0.882 0.120 8 26770511 missense variant A/G snv 0.52 0.56 5
rs375382379 0.882 0.160 5 143399792 missense variant T/C snv 4.0E-06 5
rs550659379 0.882 0.160 5 143399780 missense variant T/C snv 4.0E-06 7.0E-06 5
rs752834812 0.882 0.160 5 143399885 missense variant T/C snv 8.0E-06 5
rs772651364 0.882 0.160 5 143400050 missense variant C/T snv 4.0E-06 5