Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 10
rs1057519864
AR
0.851 0.080 X 67723707 missense variant T/C snv 8
rs976306779
AR
0.851 0.080 X 67545492 missense variant C/A;T snv 6.6E-06 8
rs864622007
AR
0.882 0.200 X 67711621 missense variant T/A snv 5
rs1340026226
AR
1.000 0.080 X 67711662 missense variant G/A snv 9.5E-06 3
rs753066745
SH3BGRL
X 81277164 missense variant C/T snv 1.7E-05 9.5E-06 2
rs1317052311
VEGFD ; PIR-FIGF
X 15358134 missense variant C/A snv 5.5E-06 1
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs1235679626
MORC2
0.925 0.080 22 30940834 missense variant C/T snv 1.4E-05 3
rs767649
MIR155HG ; MIR155
0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18
rs1056123575
ADAMTS1
0.925 0.080 21 26844557 missense variant G/A snv 4.2E-06 7.0E-06 4
rs2835931
KCNJ6
1.000 0.120 21 37749345 intron variant C/A;T snv 4
rs477145
TIAM1
1.000 0.120 21 31390097 intron variant C/A;T snv 4
rs772893086
ADARB1
0.925 0.080 21 45176099 missense variant A/C;G;T snv 4.0E-06 4
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs758272654
GNAS
0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs17577
SLC12A5-AS1 ; MMP9
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 31
rs2250889
SLC12A5-AS1 ; MMP9
0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 24
rs6024836
FAM210B ; AURKA
0.851 0.160 20 56369012 downstream gene variant G/A snv 0.42 7
rs4647958
SNAI1
0.851 0.080 20 49984094 missense variant T/C snv 0.18 0.29 5
rs2064863
AURKA
0.925 0.120 20 56387716 intron variant T/A;C;G snv 4
rs1219211410
CDC25B
0.925 0.080 20 3800494 missense variant T/C snv 3
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107