Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6911490
ATG5 ; PRDM1
1.000 0.040 6 106074152 intron variant T/C snv 0.86 1
rs28701841
ATG5 ; PRDM1
0.827 0.120 6 106082455 intron variant G/A snv 7.6E-02 5
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs12369214
RIC8B
0.807 0.120 12 106804833 intron variant G/A snv 0.41 5
rs3776414
DAP
0.827 0.120 5 10689450 intron variant T/G snv 0.48 6
rs2930047
DAP
0.925 0.040 5 10695414 intron variant T/C snv 0.49 3
rs267939
DAP
1.000 0.040 5 10752203 intron variant C/T snv 0.50 1
rs7805114 0.827 0.120 7 107809588 downstream gene variant T/A;G snv 5
rs2108225 1.000 0.040 7 107812658 downstream gene variant G/A;T snv 1
rs6466198 0.827 0.120 7 107839681 regulatory region variant A/T snv 0.68 5
rs4380874 1.000 0.040 7 107839870 intergenic variant T/A;C;G snv 2
rs4510766 1.000 0.040 7 107852344 intergenic variant A/G snv 0.36 1
rs886774 1.000 0.040 7 107854989 regulatory region variant G/A snv 0.67 1
rs4598195
LOC105375444
1.000 0.040 7 107862996 intergenic variant A/C snv 0.34 1
rs7115956
RDX ; LOC107984384
0.827 0.120 11 110085620 intron variant C/T snv 0.38 5
rs4561177
RDX ; ZC3H12C
0.807 0.120 11 110091706 intron variant A/G snv 0.36 6
rs8061882
CLEC16A
0.827 0.120 16 11067551 intron variant G/C snv 0.11 5
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs3851228
LOC107986522 ; TRAF3IP2-AS1
0.925 0.040 6 111526988 intron variant A/T snv 9.7E-02 3
rs11649613
LOC107984859
0.827 0.120 16 11225500 downstream gene variant C/T snv 0.37 5
rs2024092
SBNO2
0.827 0.120 19 1124032 intron variant G/A snv 0.24 0.26 6
rs367569
LOC105371082 ; RMI2
0.807 0.120 16 11271643 intron variant C/T snv 0.32 6
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25