Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143101792
CRP
0.851 0.320 1 159714026 stop gained G/C snv 8.8E-05 1.3E-04 5
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs1979277 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs1799969 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs2250889 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 24
rs763361 0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs1143679 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs3733197 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs1805034 0.742 0.360 18 62360008 missense variant C/T snv 0.54 0.56 12
rs2073498 0.763 0.280 3 50332115 missense variant C/A snv 9.6E-02 8.0E-02 12