Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1574560 1.000 0.120 3 166329716 intergenic variant T/C snv 0.42 1
rs1614627 1.000 0.120 1 20620263 downstream gene variant A/C snv 0.86 1
rs7230264 1.000 0.120 18 27347470 intron variant G/A snv 0.15 1
rs8044477 1.000 0.120 16 58942687 intron variant A/G snv 0.53 1
rs9283636 1.000 0.120 3 166315136 intergenic variant G/A snv 0.46 1
rs9787692 1.000 0.120 10 8603200 intergenic variant T/G snv 0.30 1
rs115344852
GPX6
1.000 0.120 6 28518321 intron variant A/C snv 1
rs17130142
PKN2-AS1
1.000 0.120 1 87773925 intron variant G/A snv 6.5E-02 1
rs12039431
RSPO1
1.000 0.120 1 37616450 intron variant G/A snv 0.24 0.21 1
rs1017134 0.925 0.120 7 35307237 intergenic variant G/A snv 0.47 2
rs1192691 0.925 0.120 10 36880367 regulatory region variant G/T snv 0.90 2
rs142091544 0.925 0.120 5 168286995 upstream gene variant C/T snv 2.1E-02 2
rs4286604 0.925 0.120 4 69576447 intron variant A/G snv 0.76 2
rs7501462 0.925 0.120 17 16974091 upstream gene variant A/G snv 0.31 2
rs1955513
AKAP6
0.925 0.120 14 32706736 intron variant T/G snv 0.11 2
rs927062
AKAP6
0.925 0.120 14 32625843 intron variant A/G snv 0.22 2
rs10788679
ARHGEF10L
0.925 0.120 1 17590467 intron variant A/G snv 0.59 2
rs2256787
ARHGEF10L
0.925 0.120 1 17566321 intron variant A/C snv 0.93 2
rs7572644
BABAM2
0.925 0.120 2 28097166 intron variant T/C snv 0.21 2
rs9609538
BPIFC ; RTCB
0.925 0.120 22 32413845 upstream gene variant T/C snv 0.34 2
rs1983383
CAPN13
0.925 0.120 2 30754766 intron variant C/A snv 0.39 2
rs41324349
CARD11
0.925 0.120 7 2907529 intron variant G/A;C;T snv 2
rs3769827
CASP8
0.925 0.120 2 201237962 intron variant A/G snv 0.42 2
rs17507066
CHEK2
0.925 0.120 22 28696732 intron variant C/T snv 7.0E-02 2
rs1413299
COL15A1
0.925 0.120 9 98998959 intron variant G/A;T snv 2