Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1043307 0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1337503417 0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 12
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs146052672 0.851 0.160 6 34242693 intron variant -/C delins 5
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs1801058 0.882 0.120 4 3037423 missense variant T/C;G snv 0.62 4
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs183433761 0.851 0.200 2 162152278 5 prime UTR variant T/C;G snv 5
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs2228611 0.708 0.520 19 10156401 synonymous variant T/A;C snv 0.52 19
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs2289277 1.000 0.080 5 111073369 5 prime UTR variant C/A;G;T snv 3