Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs12218 0.763 0.280 11 18269774 synonymous variant T/C snv 0.42 0.36 11
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1975514 13 110176544 intron variant T/C;G snv 0.36; 4.0E-06 1
rs3825807 0.807 0.120 15 78796769 missense variant A/G snv 0.34 0.33 10
rs3794624 0.882 0.120 16 88650666 intron variant G/A snv 0.26 0.29 4
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs5985 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs4961 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs2296172 1.000 0.080 1 39370145 missense variant A/G;T snv 0.19; 8.0E-06 4
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1801239 0.827 0.160 10 16877053 missense variant T/C;G snv 8.9E-02; 8.0E-06 8
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11466653 1.000 0.080 4 38774614 missense variant A/G snv 6.4E-02 4.1E-02 3
rs1801177
LPL
0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 14
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs121909613
FGA
0.882 0.160 4 154585712 splice acceptor variant G/A;C;T snv 4.8E-05; 4.0E-06 5
rs552953108
F2
0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 16
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 40
rs767830104 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs1194897557 0.827 0.240 1 11796276 missense variant A/G snv 8.0E-06 7
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65