Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10484554 0.807 0.200 6 31306778 intron variant C/T snv 0.12 8
rs10484560 1.000 0.120 6 32330360 intron variant G/A snv 8.6E-02 1
rs10484565 0.925 0.200 6 32827255 3 prime UTR variant G/A snv 6.1E-02 2
rs10484566 0.925 0.200 6 32867481 regulatory region variant T/G snv 6.8E-02 2
rs10488631 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs10489629 0.827 0.240 1 67222666 intron variant T/C snv 0.48 1
rs1049281 1.000 0.120 6 31268790 3 prime UTR variant T/C snv 0.68 1
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 2
rs1050152 0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 1
rs1051336 0.925 0.120 6 32444815 3 prime UTR variant G/A;C snv 0.15 1
rs10516487 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 2
rs1051794 0.925 0.120 6 31411332 missense variant G/A snv 0.34 0.35 4
rs1052248 1.000 0.120 6 31588804 3 prime UTR variant T/A snv 0.26 1
rs1055569 0.882 0.240 6 31472305 non coding transcript exon variant C/T snv 0.41 2
rs1059288 0.882 0.320 6 33299895 3 prime UTR variant A/G snv 0.60 1
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 1
rs1063355 0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56 2
rs1063635 1.000 0.120 6 31412154 missense variant G/A snv 0.50 0.54 1
rs1075496
NRM
0.882 0.160 6 30690462 intron variant C/A snv 0.47 1
rs1076828 1.000 0.120 6 30660475 non coding transcript exon variant G/A snv 0.29 1
rs1076832 1.000 0.120 6 30452054 non coding transcript exon variant C/A snv 0.15 1
rs1077393 0.882 0.200 6 31642752 non coding transcript exon variant A/G snv 0.44 3
rs10774624 0.882 0.160 12 111395984 intron variant G/A snv 0.67 1
rs10790268 1.000 0.120 11 118858682 intergenic variant A/G;T snv 1
rs10795791 0.925 0.200 10 6066377 upstream gene variant A/G snv 0.40 1