Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs150924946 0.882 0.120 1 156135271 missense variant A/G snv 4.8E-04 1.6E-04 5
rs1559279177
HJV
0.851 0.160 1 146018661 frameshift variant G/- del 5
rs1967017 0.882 0.160 1 145711421 upstream gene variant A/G snv 0.43 5
rs2275558 0.882 0.200 1 164559883 missense variant G/A snv 0.30 0.19 5
rs3789678
AGT
1.000 0.040 1 230713736 intron variant C/T snv 0.15 5
rs60662302 0.882 0.200 1 156138593 missense variant G/A snv 2.1E-04 7.7E-04 5
rs6681231 0.882 0.120 1 186690727 intergenic variant G/C snv 0.22 5
rs7212 0.851 0.120 1 145992816 3 prime UTR variant G/C snv 0.16 5
rs758564400
REN
0.925 0.120 1 204156683 missense variant A/G snv 4.0E-06 5
rs10489177 0.925 0.120 1 169793666 missense variant T/A;G snv 4.1E-06; 0.19 4
rs1298417395 0.882 0.080 1 176206716 missense variant C/T snv 1.4E-05 4
rs1553769428
HJV
0.925 0.120 1 146018352 stop gained C/A snv 4
rs161810 0.925 0.120 1 7940737 intron variant T/C snv 0.13 4
rs7528153 0.925 0.080 1 107765105 missense variant T/A snv 0.58 0.64 4
rs7533564 0.925 0.120 1 78360228 intron variant C/T snv 0.92 4
rs755725121 0.882 0.080 1 9716029 missense variant G/A snv 2.1E-05 7.0E-06 4
rs12144939
CFH
0.925 0.080 1 196729815 intron variant G/A;T snv 3
rs17106184 0.925 0.080 1 50444313 intron variant G/A snv 8.5E-02 3
rs200879349 0.925 0.240 1 169468804 missense variant T/G snv 5.2E-05 6.3E-05 3
rs2146727 0.925 0.080 1 167312910 intron variant G/A snv 0.56 3
rs2228146 0.925 0.120 1 154454574 missense variant G/A snv 1.3E-02; 4.0E-06 5.4E-02 3
rs2275703 0.925 0.080 1 160195305 intron variant A/C snv 0.38 3
rs3767140 1.000 0.080 1 21888152 intron variant C/A snv 0.25 3
rs3767434 0.925 0.080 1 167401914 intron variant T/C snv 0.14 3
rs7539020
AGT
1.000 0.040 1 230713444 intron variant C/T snv 0.43 3