Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs603424 1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs7200543 16 15036113 synonymous variant A/G snv 0.35 0.30 6
rs4453795 3 192376186 intron variant A/G;T snv 2
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 12
rs2911711 0.925 0.120 2 27527679 downstream gene variant T/A snv 0.58 6
rs4666002 0.925 0.120 2 27617773 intron variant G/A;C snv 6
rs4775041 1.000 0.040 15 58382496 intron variant G/C snv 0.24 8
rs10468017 0.851 0.120 15 58386313 intron variant C/T snv 0.24 12
rs10517480 4 59883111 intergenic variant A/T snv 0.27 2
rs650436 11 61768958 intron variant C/T snv 0.39 2
rs579383 11 61769111 intron variant G/A snv 0.58 2
rs2269928 11 61770057 intron variant T/G snv 0.18 2
rs149803 11 61771548 synonymous variant C/G;T snv 0.18 2
rs174528 1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 5
rs108499 11 61779765 intron variant C/T snv 0.27 2
rs509360 11 61781087 intron variant A/G snv 0.61 0.52 3
rs174532 11 61781402 intron variant G/A snv 0.20 2
rs174534 1.000 0.080 11 61781986 non coding transcript exon variant A/G snv 0.28 3
rs174535 0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs174536 11 61784455 non coding transcript exon variant A/C snv 0.29 3
rs17762402 11 61785729 intron variant G/A snv 4.8E-02 2
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18