Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34811474 1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs1126464 1.000 0.040 16 89637957 missense variant G/A;C snv 1.3E-05; 0.26 4
rs1940475 1.000 0.040 11 102722517 missense variant T/C;G snv 0.54 4
rs2908004 1.000 0.040 7 121329715 missense variant G/A;T snv 0.44; 4.0E-06 4
rs1042667 1.000 0.040 17 72124410 3 prime UTR variant A/C snv 0.41 0.36 3
rs3830675 1.000 0.040 10 87931195 intron variant -/TCTTA delins 3
rs10654220 1.000 0.040 12 123218875 intron variant -/TGT;TGTTGT delins 2
rs1905786 1.000 0.040 8 118939453 intron variant T/A;C snv 2
rs2830585 1.000 0.040 21 26932893 missense variant C/T snv 0.12 0.12 2
rs4072286 1.000 0.040 8 141726333 regulatory region variant G/A;T snv 2
rs4721 1.000 0.040 7 150338437 missense variant T/A;C;G snv 0.42 0.47 2
rs6773957 1.000 0.040 3 186855916 3 prime UTR variant A/C;G snv 0.55 2
rs919642 1.000 0.040 9 114148867 intergenic variant A/T snv 0.22 2
rs10172410 1.000 0.040 2 181487841 intron variant T/C snv 0.45 1
rs10218792 1.000 0.040 1 245587630 intron variant T/G snv 0.26 1
rs1032128 1.000 0.040 8 118939534 intron variant G/A snv 0.30 1
rs1034762 1.000 0.040 12 47995860 intron variant A/C snv 0.74 0.79 1
rs10401670 1.000 0.040 19 7677916 intron variant T/C;G snv 0.49 1
rs10502437 1.000 0.040 18 23390742 intron variant G/A snv 0.30 1
rs1052981 1.000 0.040 7 37906899 3 prime UTR variant G/A snv 0.70 1
rs1062033 1.000 0.040 15 51255741 5 prime UTR variant C/G snv 0.35 1
rs10795550 1.000 0.040 10 7562392 3 prime UTR variant T/C;G snv 0.88 1
rs10948155 1.000 0.040 6 44720220 intergenic variant T/C snv 0.30 1
rs10980705 1.000 0.040 9 111040905 upstream gene variant C/T snv 0.18 1
rs11031191 1.000 0.040 11 30752733 intergenic variant G/C;T snv 0.27 1