Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 7
rs8040868 0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 7
rs1057518913 0.851 0.320 9 137762822 splice donor variant T/C snv 7
rs9272535 0.827 0.280 6 32638979 synonymous variant G/A snv 3.0E-05 1.8E-03 7
rs2710323 0.851 0.080 3 52781889 intron variant T/C snv 0.49 0.54 7
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs389883 0.827 0.200 6 31979683 non coding transcript exon variant G/T snv 0.80 6
rs17514846 0.882 0.120 15 90873320 intron variant C/A;G snv 6
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs3131296 0.807 0.320 6 32205216 intron variant C/T snv 0.11 6
rs2252865 0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs9371601 0.790 0.120 6 152469438 intron variant G/T snv 0.46 6
rs12576775 0.827 0.080 11 79366149 intron variant A/G snv 0.15 6
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs12871532 0.851 0.040 13 108016199 intergenic variant T/C snv 0.46 5
rs13072940 0.851 0.040 3 36801132 regulatory region variant T/A snv 0.37 5
rs13418455 0.851 0.040 2 180212022 intergenic variant C/T snv 0.29 5
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 5
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 5
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
rs10994359 0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 5