Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10074991 0.851 0.120 5 40790449 intron variant G/A snv 0.31 7
rs1016343 0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20 8
rs1042028 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs1047972 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs10739971 0.882 0.080 9 94175398 intron variant G/A;C snv 5
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs11187842 0.925 0.080 10 94292754 intron variant C/T snv 7.8E-02 5
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1131445 0.724 0.440 15 81309441 3 prime UTR variant T/A;C snv 16
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs11536889 0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62