Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10636 0.851 0.160 16 56609431 3 prime UTR variant G/C snv 0.26 7
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs11196172 0.708 0.200 10 112967084 intron variant G/A snv 0.13 18
rs11212617 0.827 0.200 11 108412434 intron variant C/A snv 0.49 7
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11915160 0.851 0.200 3 181713783 3 prime UTR variant C/A snv 0.11 5
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs12325817 0.807 0.320 17 17583205 intron variant C/A;G;T snv 7
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1520220 0.807 0.280 12 102402744 intron variant G/C;T snv 0.76 9
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs16917496 0.689 0.360 12 123409283 3 prime UTR variant C/G;T snv 21
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113