Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 10
rs11646213 0.827 0.320 16 82609046 intergenic variant A/T snv 0.47 6
rs12449782 0.925 0.200 17 63498888 intron variant G/A snv 0.41 3
rs16835198 0.882 0.200 1 32861080 downstream gene variant G/T snv 0.29 3
rs955333 0.882 0.240 6 154626274 intergenic variant A/G snv 0.13 3
rs10255208 0.925 0.160 7 36819038 non coding transcript exon variant A/G snv 0.46 2
rs17300593 0.925 0.160 1 58637536 intergenic variant C/G snv 2
rs1942872 0.925 0.160 18 60201132 downstream gene variant C/T snv 0.21 2
rs2874116 0.925 0.160 18 58792367 regulatory region variant G/A snv 0.36 2
rs488846 0.925 0.160 18 54261400 intergenic variant T/C snv 0.26 2
rs499765 0.925 0.160 19 48763133 downstream gene variant C/G snv 0.45 2
rs6704078 0.925 0.200 1 216437370 intergenic variant C/T snv 0.94 2
rs9942471 0.925 0.160 6 89238513 intergenic variant A/C snv 0.37 2
rs10952362 1.000 0.120 7 152565713 regulatory region variant T/C snv 0.25 1
rs11886047 1.000 0.120 2 43623451 upstream gene variant T/A;C snv 0.20 1
rs1249910 1.000 0.120 3 112672327 intergenic variant A/G snv 0.58 1
rs12523822 1.000 0.120 6 154633286 intergenic variant C/G;T snv 1
rs1253192 1.000 0.120 14 59376688 intergenic variant A/G snv 0.92 1
rs16996381 1.000 0.120 22 36115231 intergenic variant G/A snv 0.31 1
rs1866813 1.000 0.120 3 137083096 intergenic variant A/C snv 0.14 1
rs334543 1.000 0.120 3 120113774 intron variant C/A snv 0.74 1
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29
rs2268388
ACACB
0.851 0.200 12 109205840 intron variant G/A snv 0.14 6