Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3781094
GATA3
1.000 0.120 10 8059464 intron variant A/C snv 0.52 2
rs9603608
COG6
13 39744682 intron variant A/C snv 0.30 1
rs35621564 1.000 0.080 7 20547220 regulatory region variant A/C;G snv 2
rs7170165
ADAMTSL3
15 83878087 intron variant A/C;G snv 1
rs2390314 0.925 0.120 7 20416355 downstream gene variant A/C;T snv 3
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 5
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 4
rs36045143
LOC105371081 ; CLEC16A
1.000 0.080 16 11131109 intron variant A/G snv 0.18 3
rs7734635 0.925 0.080 5 110823145 intergenic variant A/G snv 0.30 3
rs912131
UBAC2
13 99380092 intron variant A/G snv 0.57 2
rs112068732 17 40204213 regulatory region variant A/G snv 3.9E-02 1
rs11567694
IL7R ; LOC105374724
5 35857602 intron variant A/G snv 0.25 1
rs3744787
CEP295NL ; TIMP2
17 78897589 non coding transcript exon variant A/G snv 0.28 1
rs75567729
PTPRC
1 198641406 intron variant A/G snv 8.4E-02 1
rs13099273
LPP
1.000 0.080 3 188415730 intron variant A/G;T snv 2
rs6011033
RTEL1-TNFRSF6B ; RTEL1
20 63691346 intron variant A/G;T snv 2
rs7626218
TBL1XR1
0.925 0.080 3 177134250 intron variant A/T snv 0.41 3
rs72833417 1.000 0.080 17 47795683 intergenic variant A/T snv 9.7E-02 2
rs5743618
TLR1
0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 6
rs117710327 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 5
rs159963
RERE
1.000 0.040 1 8444361 intron variant C/A snv 0.52 3
rs16903574
OTULINL
0.882 0.120 5 14610200 missense variant C/A;G snv 4.0E-06; 5.6E-02 6
rs10036789 1.000 0.080 5 72400091 regulatory region variant C/A;G snv 3
rs2497318 0.827 0.120 10 92672243 upstream gene variant C/A;T snv 6
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv 6