Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs2523987 0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 5
rs1517352 0.851 0.160 2 191066738 intron variant A/C snv 0.45 3
rs437179 0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78 3
rs630379 0.882 0.200 6 31954477 intron variant A/C snv 0.77 0.79 3
rs6568431 0.790 0.320 6 106140931 intron variant A/C snv 0.61 2
rs10489265 0.827 0.200 1 173266926 regulatory region variant A/C snv 0.21 1
rs10498070 0.925 0.080 2 219833404 intergenic variant A/C snv 0.39 1
rs1419183 1.000 0.080 6 28275017 intron variant A/C snv 0.17 1
rs6659932 0.827 0.240 1 67336688 intron variant A/C snv 0.81 1
rs7172677 0.925 0.080 15 75132252 intergenic variant A/C snv 0.71 1
rs729302 0.827 0.160 7 128928906 intergenic variant A/C snv 0.28 1
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs12531711 0.827 0.200 7 128977412 intron variant A/C;G snv 2
rs12720356 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 2
rs1893592 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 2
rs280519 0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 2
rs10946940 1.000 0.080 6 27592808 upstream gene variant A/C;G snv 1
rs1382568
BLK
0.925 0.160 8 11493711 intron variant A/C;G snv 1
rs3130342 1.000 0.080 6 32112369 non coding transcript exon variant A/C;G;T snv 1
rs2618444 0.925 0.160 8 11480861 intron variant A/C;T snv 1
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs389884 0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 7
rs11229 0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
rs1235162 0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6