Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3900940 0.827 0.040 3 108428881 missense variant T/A;C snv 4.3E-06; 0.24 6
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
rs1122608 0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs147377392 0.763 0.120 20 23048144 missense variant A/G snv 1.0E-04 2.8E-04 11
rs532019808 0.827 0.120 11 89451807 missense variant G/A;C snv 4.0E-06; 4.0E-06 8
rs20455 0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs2277680 0.776 0.160 17 4735268 missense variant G/A snv 0.47 0.41 10
rs5182 0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs775381348 0.807 0.160 14 35308023 missense variant G/T snv 8
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs1799998 0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs9797861 0.790 0.200 19 10632450 intron variant C/A;G;T snv 9
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs146292819 0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04 9
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs201058276
F7
0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 11
rs2288904 0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 8
rs5065 0.763 0.240 1 11846011 stop lost A/G snv 0.14 0.21 12
rs11053646 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs12190287 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 19
rs1333040 0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15