Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1122608 0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs281865545 0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs999947969 0.827 0.080 7 80671145 synonymous variant C/T snv 7
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs767830104 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs770572030 0.827 0.160 18 49581427 missense variant T/A;C snv 4.0E-06; 4.0E-06 5
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs771676129 0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 7
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs201058276
F7
0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 11
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53