Disease: Exudative age-related macular degeneration
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs1626340 0.827 0.120 9 99161090 intergenic variant G/A;T snv 5
rs201459901 0.851 0.040 20 58078668 regulatory region variant -/A delins 0.21 4
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs61818925 0.851 0.040 1 196846320 upstream gene variant T/G snv 0.67 4
rs72802342 0.851 0.040 16 75200974 downstream gene variant C/A snv 6.2E-02 5
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs57137919
ABCG1 ; LOC105372814
0.776 0.160 21 42218908 intron variant G/A snv 0.14 9
rs61941274
ACAD10
0.827 0.160 12 111694806 intron variant G/A;T snv 5
rs62247658
ADAMTS9-AS2
0.851 0.040 3 64729479 intron variant C/T snv 0.42 4
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54 9
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs12357257
ARHGAP21
0.851 0.040 10 24710664 intron variant G/A snv 0.18 4
rs10490924
ARMS2 ; LOC105378525
0.716 0.240 10 122454932 missense variant G/T snv 0.26 0.23 16
rs2736911
ARMS2 ; LOC105378525
0.882 0.120 10 122454839 stop gained C/A;T snv 4.0E-06; 0.13 3
rs3750846
ARMS2 ; LOC105378525
0.851 0.040 10 122456049 intron variant T/C snv 0.24 4
rs9564692
B3GLCT
0.851 0.040 13 31247103 splice region variant C/T snv 0.40 0.36 4
rs147859257
C3
0.827 0.040 19 6718135 missense variant T/G snv 2.8E-03 2.4E-03 6
rs2230199
C3
0.763 0.240 19 6718376 missense variant G/C;T snv 0.15 10
rs6982567
C8orf37-AS1
0.882 0.040 8 95738053 intron variant C/T snv 0.24 3
rs62358361
C9
0.851 0.040 5 39327786 intron variant G/C;T snv 5