Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11781551 1.000 0.040 8 122395852 intergenic variant G/A snv 0.40 1
rs118204057
LPL
0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 16
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
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
rs121918313 0.851 0.080 12 12164494 missense variant G/A snv 1.6E-05 4
rs121918393 0.851 0.120 19 44908756 missense variant C/A;T snv 1.3E-05; 9.0E-05 6
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs12347433 0.882 0.040 9 115035318 synonymous variant T/C snv 0.23 0.21 3
rs1249040838 0.827 0.120 19 11113699 missense variant G/A snv 4.0E-06 5
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs12564445 0.851 0.040 1 201376359 intron variant G/A snv 0.27 5
rs1264352930 0.807 0.120 11 116836082 missense variant C/A snv 4.2E-06 6
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs12762303 0.851 0.080 10 45373723 upstream gene variant T/C snv 0.17 4
rs1282382243 0.807 0.120 13 50843630 missense variant G/A snv 8
rs12953 0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 9
rs1298417395 0.882 0.080 1 176206716 missense variant C/T snv 1.4E-05 4
rs1314386070 0.827 0.240 8 90042766 missense variant T/C snv 1.4E-05 9
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs13447720 0.925 0.040 11 94432160 intron variant T/C snv 0.17 2
rs1346044
WRN
0.708 0.440 8 31167138 missense variant T/C snv 0.24 0.23 23
rs137852912 0.776 0.120 1 55057454 missense variant G/A;C;T snv 7.2E-05 10
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs138227502 0.925 0.040 3 186853221 missense variant C/T snv 1.8E-04 5.6E-04 2