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
rs59834205
SLC2A9
0.882 0.200 4 9959396 intron variant -/GA delins 1.1E-04 3
rs1539019
NLRP3
0.882 0.240 1 247436999 intron variant A/C snv 0.63 6
rs1150660 0.925 0.120 6 26101212 upstream gene variant A/C snv 0.73 5
rs13023094
SLC4A1AP
0.925 0.120 2 27687839 intron variant A/C snv 0.16 4
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
rs9358903 0.925 0.120 6 26061721 intergenic variant A/C snv 0.38 4
rs9467636
SLC17A2
0.925 0.120 6 25919321 intron variant A/C snv 0.34 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
rs12201186 0.925 0.120 6 25625367 downstream gene variant A/C snv 0.28 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
rs8179252
GCKR
0.882 0.120 2 27523965 downstream gene variant A/C snv 0.37 3