Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2079742
BCAS3
0.851 0.240 17 61388336 non coding transcript exon variant T/C snv 0.20 9
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 9
rs17050272
LOC105373585
0.882 0.120 2 120548864 upstream gene variant G/A snv 0.33 9
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 9
rs1478604
THBS1
0.807 0.240 15 39581120 5 prime UTR variant T/C snv 0.40 9
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 8
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs963837
LOC101928338 ; LINC02859
0.925 0.120 11 30727543 intergenic variant T/C snv 0.35 8
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 8
rs760077
MTX1 ; THBS3
0.925 0.120 1 155208991 missense variant T/A snv 0.36 8
rs3823418
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 0.23 8
rs121907892
SLC22A12
0.807 0.240 11 64593747 stop gained G/A;C snv 2.8E-04 8
rs4014195 0.882 0.200 11 65739351 intergenic variant C/G snv 0.31 7
rs1178977
BAZ1B
0.925 0.120 7 73442719 splice region variant A/G snv 0.16 0.21 7
rs55781567
CHRNA5
0.851 0.080 15 78565644 5 prime UTR variant C/G snv 0.31 7
rs3741414
INHBC
0.925 0.120 12 57450266 3 prime UTR variant C/T snv 0.19 7
rs3925584
LOC101928338
1.000 0.080 11 30738788 intergenic variant T/C snv 0.35 7
rs77924615
PDILT
1.000 0.080 16 20381010 intron variant G/A snv 0.16 7
rs1106766
R3HDM2
0.882 0.120 12 57415673 intron variant C/T snv 0.19 7
rs1171614
SLC16A9
0.882 0.200 10 59709780 5 prime UTR variant T/C snv 0.79 7
rs16890979
SLC2A9
0.827 0.200 4 9920543 missense variant C/T snv 0.24 0.29 7
rs6855911
SLC2A9
0.851 0.200 4 9934286 intron variant A/G snv 0.33 7
rs734553
SLC2A9
0.851 0.240 4 9921380 intron variant G/A;T snv 7
rs737267
SLC2A9
0.851 0.240 4 9933120 intron variant G/A;T snv 7
rs6449213
SLC2A9 ; LOC105374476
0.827 0.240 4 9992591 intron variant C/T snv 0.82 7