Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1010 0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
rs10118757 0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs11053646 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs11066001 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs1122608 0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs112735431 0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
rs11542041 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12190287 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 19
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1333040 0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60