Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16991615
MCM8
0.925 0.080 20 5967581 missense variant G/A snv 4.5E-02 4.2E-02 6
rs6569648
L3MBTL3
1.000 0.080 6 130027974 intron variant C/T snv 0.84 5
rs569550
LSP1
0.925 0.080 11 1865838 intron variant T/G snv 0.35 4
rs7166081 0.925 0.080 15 67199963 downstream gene variant G/A snv 0.76 4
rs7223535
ATAD5
1.000 0.080 17 30884649 intron variant G/A snv 0.25 4
rs117758012
HOOK2 ; MAST1
1.000 0.080 19 12846836 intron variant C/T snv 4.1E-02 3
rs1858826
GNGT1
1.000 0.080 7 93719703 intron variant C/T snv 0.90 3
rs1973765
LSP1
1.000 0.080 11 1877434 intron variant T/C snv 0.37 3
rs3741378
SIPA1
0.851 0.080 11 65641466 missense variant C/G;T snv 0.15 3
rs3755967
GC
0.925 0.080 4 71743681 intron variant C/A;T snv 3
rs592373
LSP1
0.925 0.080 11 1869760 intron variant G/A;T snv 0.63; 6.8E-06 3
rs72755295
EXO1
1.000 0.080 1 241870961 intron variant A/G snv 2.1E-02 3
rs10771399 0.827 0.080 12 28002147 intergenic variant A/G snv 8.9E-02 2
rs111342015
TTBK1
1.000 0.080 6 43259403 intron variant G/A;T snv 2
rs113701136 1.000 0.080 19 29786822 intergenic variant C/T snv 0.26 2
rs114971217 0.925 0.080 2 236525150 intergenic variant T/A;C snv 2
rs11651604 0.925 0.080 17 71440368 regulatory region variant G/A;C snv 2
rs117114682
PTPRN2
0.925 0.080 7 158170200 intron variant A/G snv 2.6E-02 2
rs12286929 0.925 0.080 11 115151684 intergenic variant A/C;G snv 2
rs12422552 0.925 0.080 12 14260997 regulatory region variant G/C snv 0.30 2
rs13260300 1.000 0.080 8 74567389 regulatory region variant C/T snv 0.67 2
rs13431652
SPC25
0.925 0.080 2 168896905 intron variant T/C snv 0.24 2
rs1353747
PDE4D
0.882 0.080 5 59041654 intron variant T/G snv 6.9E-02 2
rs147512482 0.925 0.080 22 27215781 intergenic variant C/G snv 2.4E-03 2
rs1519277 0.925 0.080 2 123261223 intergenic variant C/T snv 0.12 2