Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7213516 0.882 0.080 17 63474189 upstream gene variant G/A snv 5.7E-02 3
rs9974610 1.000 0.080 21 31646056 intergenic variant A/G snv 0.13 3
rs11748327 1.000 0.080 5 4029676 downstream gene variant C/T snv 0.21 2
rs1395479 1.000 0.080 4 177397037 intergenic variant C/A;T snv 2
rs1722842 0.925 0.080 15 23785809 intron variant T/C snv 0.16 2
rs2001846 1.000 0.080 8 125466208 upstream gene variant T/A;C snv 2
rs230119 1.000 0.080 9 119152945 downstream gene variant C/A;T snv 2
rs3917639 0.925 0.120 1 94527220 downstream gene variant C/T snv 2
rs4593108 0.925 0.080 4 147359849 regulatory region variant C/G snv 0.31 2
rs1008563 1.000 0.080 2 218162165 downstream gene variant G/A snv 0.43 1
rs10176176 1.000 0.080 2 85534925 upstream gene variant A/T snv 0.54 1
rs17708087 1.000 0.080 17 40514261 upstream gene variant A/G snv 0.15 1
rs2019090 1.000 0.080 11 103798234 intron variant A/C;G;T snv 1
rs2315065 1.000 0.080 6 160687112 intergenic variant C/A;T snv 1
rs490556 1.000 0.080 5 4022536 intergenic variant G/A snv 0.57 1
rs521660 1.000 0.080 5 4035819 intron variant T/C snv 0.61 1
rs6941513 1.000 0.080 6 163609768 intergenic variant A/G snv 0.45 1
rs7211079 1.000 0.080 17 80133738 downstream gene variant A/G snv 0.29 1
rs822387 1.000 0.080 3 186838248 upstream gene variant T/C snv 0.15 1
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs1239681664
ABCA1
0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs4149313
ABCA1
0.763 0.240 9 104824472 missense variant T/C snv 9
rs2230808
ABCA1
0.827 0.240 9 104800523 missense variant T/C snv 0.71 0.60 6
rs13301354
ABCA2 ; FUT7 ; C9orf139
1.000 0.080 9 137030185 3 prime UTR variant T/C snv 0.64 1