Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10801558
CFH
1.000 0.040 1 196729914 intron variant T/G snv 0.46 2
rs10801559
CFH
1.000 0.040 1 196735074 intron variant G/A snv 0.44 2
rs10922104
CFH
1.000 0.040 1 196718600 intron variant A/C;G snv 2
rs10922105
CFH
1.000 0.040 1 196721120 intron variant A/C;T snv 2
rs10922108
CFH
1.000 0.040 1 196732343 intron variant A/T snv 0.46 2
rs11118892 1.000 0.040 1 221910253 intron variant G/C;T snv 2
rs114931935 0.925 0.080 1 161690011 upstream gene variant G/A snv 3.0E-02 2
rs1329427
CFH
1.000 0.040 1 196735429 intron variant C/T snv 0.44 2
rs143262451 1.000 0.040 1 93407898 intergenic variant G/A snv 2.6E-03 2
rs144177292 1.000 0.040 1 201994931 intron variant C/T snv 2.8E-03 2
rs181020201 1.000 0.040 1 51134390 intron variant A/C snv 1.1E-04 2
rs3009947 1.000 0.040 1 218515813 intron variant T/C snv 0.47 2
rs305221 1.000 0.040 1 88733302 intron variant G/A snv 0.59 2
rs34585985 0.925 0.080 1 210316066 intergenic variant A/G snv 5.2E-02 2
rs3738676 1.000 0.040 1 39525916 3 prime UTR variant G/A;T snv 2
rs3766405
CFH
1.000 0.040 1 196726031 intron variant C/T snv 0.46 2
rs3831317 0.925 0.080 1 203217822 stop gained -/AGACCATGGCCCCGCCCAGTCCCT delins 2
rs3924223 1.000 0.040 1 221905852 intron variant G/A;C snv 2
rs4457591 1.000 0.040 1 221905258 intron variant T/C snv 0.48 2
rs59985166 1.000 0.040 1 10662447 intron variant C/T snv 4.9E-02 2
rs61781370 1.000 0.040 1 39579628 upstream gene variant A/C snv 0.17 2
rs6677089
CFH
1.000 0.040 1 196715183 intron variant A/C snv 0.46 2
rs6688272
CFH
1.000 0.040 1 196715262 intron variant G/T snv 0.44 2
rs7514261
CFH
1.000 0.040 1 196731784 intron variant G/A;T snv 2
rs10890311 1.000 0.040 1 44602096 intron variant C/T snv 0.22 1