Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2255280
C9 ; DAB2
0.925 0.120 5 39394887 intron variant C/A snv 0.98 2
rs7074891
TRDMT1
0.925 0.120 10 17146475 3 prime UTR variant C/T snv 0.95 2
rs4759314
HOTAIR
0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs1143684
NQO2
0.882 0.160 6 3010156 missense variant C/T snv 0.79 0.84 4
rs4795218
HNF1B ; LOC105371754
0.925 0.120 17 37718512 intron variant A/G snv 0.82 2
rs7503953 0.882 0.320 17 6238357 intergenic variant A/C snv 0.81 3
rs3124761
SLC2A6
0.925 0.120 9 133474633 intron variant T/C snv 0.80 2
rs2035565
LINC01829
1.000 0.120 2 67392524 intron variant C/T snv 0.74 1
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs4927850
TFRC
0.925 0.120 3 196024759 intron variant T/C snv 0.71 2
rs13303010
KLHL17 ; NOC2L
0.925 0.120 1 959193 intron variant G/A snv 0.82 0.69 2
rs2980879 0.925 0.120 8 125469233 intron variant A/T snv 0.69 3
rs1630747
SLC5A3 ; MRPS6
0.925 0.120 21 34085692 intron variant C/A snv 0.69 2
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs7993418
FLT1
0.925 0.120 13 28308924 synonymous variant G/A snv 0.80 0.67 2
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs2941471
HNF4G
0.851 0.240 8 75558169 intron variant G/A snv 0.65 4
rs1561927
LINC00824
0.807 0.280 8 128555832 intron variant C/T snv 0.65 6
rs1537373
CDKN2B-AS1
0.925 0.120 9 22103342 intron variant T/G snv 0.63 3
rs2457571
SLC22A3
0.925 0.120 6 160413796 intron variant T/C snv 0.62 2
rs9582036
FLT1
0.776 0.280 13 28311271 intron variant C/A snv 0.59 8
rs2073389
SMARCB1
0.925 0.120 22 23791306 intron variant C/T snv 0.59 2
rs5757573
PDGFB
0.925 0.120 22 39237617 intron variant C/T snv 0.57 2