Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1077773 1.000 0.040 7 17403055 intron variant G/A;C snv 2
rs10797432 1.000 0.040 1 2569899 downstream gene variant C/T snv 0.51 2
rs10800309 0.925 0.120 1 161502368 upstream gene variant A/G;T snv 2
rs111456533 1.000 0.040 10 124750812 intron variant G/A snv 0.18 2
rs11150589 1.000 0.040 16 30471173 upstream gene variant T/A;C;G snv 2
rs11548656 1.000 0.040 16 81883307 missense variant A/G snv 2.5E-02 2.7E-02 2
rs11554257 1.000 0.040 9 114842790 upstream gene variant T/C snv 0.13 2
rs11672983 1.000 0.040 19 54871595 upstream gene variant G/A snv 0.35 2
rs16940202 1.000 0.040 16 85980635 intron variant T/C snv 0.15 2
rs17229285 1.000 0.040 2 198658398 intron variant C/A;T snv 2
rs17656349 1.000 0.040 5 150226431 intron variant C/T snv 0.45 2
rs1811711 1.000 0.040 2 227805760 5 prime UTR variant C/A;G snv 2
rs2395128 1.000 0.040 10 75052692 intron variant G/T snv 0.32 2
rs254560 1.000 0.040 5 135107916 intron variant G/A snv 0.32 2
rs2651244 1.000 0.040 1 70529879 upstream gene variant G/A snv 0.30 2
rs3116494 0.882 0.120 2 203727298 intron variant G/A snv 0.76 2
rs35675666 1.000 0.040 1 7961913 5 prime UTR variant G/C;T snv 2
rs4380874 1.000 0.040 7 107839870 intergenic variant T/A;C;G snv 2
rs4676408 1.000 0.040 2 240634984 downstream gene variant G/A;T snv 0.57 2
rs4743820 1.000 0.040 9 91166134 non coding transcript exon variant C/T snv 0.61 2
rs483905 1.000 0.040 11 96290263 intron variant G/A snv 0.26 2
rs501916 1.000 0.040 15 47761032 synonymous variant C/A snv 0.40 0.41 2
rs561722 1.000 0.040 11 114516108 upstream gene variant C/T snv 0.35 2
rs6017342 0.925 0.120 20 44436388 non coding transcript exon variant A/C snv 0.62 2
rs6927022 1.000 0.040 6 32644620 non coding transcript exon variant A/G snv 0.42 2