Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4910623 0.925 0.040 11 4368409 upstream gene variant G/A;T snv 2
rs12661281 0.882 0.040 6 31874821 missense variant T/A snv 0.15 0.11 3
rs1999930
FRK
0.882 0.040 6 116065971 intergenic variant C/A;G;T snv 3
rs2284665 0.882 0.040 10 122467114 intron variant G/A;T snv 3
rs2285714 0.882 0.040 4 109717654 synonymous variant C/T snv 0.37 0.31 3
rs2736911 0.882 0.120 10 122454839 stop gained C/A;T snv 4.0E-06; 0.13 3
rs3793917 0.882 0.040 10 122459759 non coding transcript exon variant C/G snv 0.23 3
rs4711751 0.882 0.040 6 43860845 intergenic variant T/C snv 0.37 3
rs6982567 0.882 0.040 8 95738053 intron variant C/T snv 0.24 3
rs10781182 0.851 0.040 9 74002804 intergenic variant T/G snv 0.54 4
rs114092250 0.851 0.040 5 35494346 intergenic variant G/A;T snv 4
rs11884770 0.851 0.040 2 227222204 intron variant T/A;C snv 4
rs12019136 0.851 0.040 19 5835666 intron variant G/A snv 0.12 4
rs12357257 0.851 0.040 10 24710664 intron variant G/A snv 0.18 4
rs140647181 0.851 0.040 3 99461824 intergenic variant T/C snv 1.5E-02 4
rs142450006 0.851 0.040 20 45986353 regulatory region variant TTCT/-;TTCTTTCT delins 2.0E-02 4
rs148553336 0.851 0.040 1 196644043 intergenic variant T/C snv 7.7E-03 4
rs181705462 0.851 0.040 6 31979250 intron variant G/C;T snv 4
rs187328863 0.851 0.040 1 196411028 intron variant C/T snv 1.6E-02 4
rs191281603 0.851 0.040 1 196989521 intron variant C/G;T snv 4.6E-03 4
rs201459901 0.851 0.040 20 58078668 regulatory region variant -/A delins 0.21 4
rs2842339 0.851 0.040 14 68520282 intron variant G/A snv 0.90 4
rs35292876
CFH
0.851 0.040 1 196737512 synonymous variant C/T snv 1.0E-02 8.6E-03 4
rs3750846 0.851 0.040 10 122456049 intron variant T/C snv 0.24 4
rs3750847 0.882 0.040 10 122455905 intron variant C/T snv 0.23 4