Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs200251830
WDR1
0.925 0.120 4 10073861 upstream gene variant -/AT delins 3
rs35385468 0.925 0.120 6 26101212 upstream gene variant -/C delins 9.7E-03 5
rs386406569 0.925 0.120 6 26101212 upstream gene variant -/C delins 5
rs577259500 0.925 0.120 4 10136132 intergenic variant -/C;CC ins 3
rs1150660 0.925 0.120 6 26101212 upstream gene variant A/C snv 0.73 5
rs626277
DACH1
1.000 0.080 13 71773564 intron variant A/C snv 0.51 5
rs3114018
ABCG2
0.882 0.160 4 88143429 intron variant A/C snv 0.48 4
rs3804105
CARMIL1
0.925 0.120 6 25612455 intron variant A/C snv 0.29 4
rs1165189
SLC17A3
0.925 0.120 6 25849551 intron variant A/C snv 0.25 3
rs11728055 0.925 0.120 4 10294674 non coding transcript exon variant A/C snv 5.2E-02 3
rs13125209
SLC2A9
0.925 0.120 4 9980420 intron variant A/C snv 0.71 3
rs17246501
SLC2A9
0.925 0.120 4 9984086 intron variant A/C snv 0.42 3
rs2728132
PKD2
0.925 0.120 4 88061309 intron variant A/C snv 0.31 3
rs4619888 0.925 0.120 4 10125354 intergenic variant A/C snv 0.18 3
rs4697693
SLC2A9
0.925 0.120 4 9894236 intron variant A/C snv 0.25 3
rs6853659 0.925 0.120 4 10350346 intergenic variant A/C snv 0.25 3
rs6857135 0.925 0.120 4 10368961 intergenic variant A/C snv 0.62 3
rs714436 0.925 0.120 4 10313043 intergenic variant A/C snv 0.17 3
rs7435196
SLC2A9
0.925 0.120 4 9965932 intron variant A/C snv 0.51 3
rs887731 0.925 0.120 4 10181562 regulatory region variant A/C snv 0.65 3
rs993172 0.925 0.120 4 10322737 intergenic variant A/C snv 0.44 3
rs7212936
SERPINF2
17 1743357 intron variant A/C snv 0.46 2
rs11070231
FSIP1
15 39729375 intron variant A/C snv 0.44 1
rs12484795
PNPLA3
22 43947746 intron variant A/C snv 0.21 1
rs1649078
BICC1
10 58533560 intron variant A/C snv 0.45 1