Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs2234767 0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 30
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs7775 0.732 0.240 2 182834857 missense variant G/A;C;T snv 8.0E-05; 8.0E-02; 5.6E-05 14
rs419598 0.742 0.280 2 113129630 synonymous variant T/C snv 0.26 0.21 13
rs1456315 0.790 0.200 8 127091692 non coding transcript exon variant T/A;C snv 9