Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs2056625
CD247
0.925 0.080 1 167451062 intron variant G/A snv 0.27 2
rs301817
RERE
0.925 0.120 1 8443319 intron variant C/A;G;T snv 2
rs3748816
MMEL1
0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 2
rs61815704 1.000 0.080 1 152921415 intergenic variant C/G snv 1.1E-02 2
rs61816766
FLG-AS1
1.000 0.080 1 152347096 intron variant T/C snv 1.6E-02 2
rs67551275
SPSB1
0.925 0.080 1 9296617 intron variant T/C snv 0.43 2
rs742230
RUNX3 ; LOC107984932
1.000 0.080 1 24924933 intron variant G/A snv 0.53 2
rs7521681
VAV3
0.925 0.120 1 107779913 intron variant G/A snv 0.15 2
rs76181804 0.925 0.120 1 198632575 intergenic variant A/G snv 8.2E-02 2
rs903361
ADORA1
0.882 0.160 1 203122146 intron variant G/A;C snv 2
rs10399805
CHI3L1
0.851 0.240 1 203186870 upstream gene variant G/A;T snv 1
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 1
rs1101999
PYHIN1
1.000 0.080 1 158962765 intron variant C/T snv 0.92 1
rs11121240
RERE
1.000 0.080 1 8834298 intron variant A/T snv 0.51 1
rs11240285 1.000 0.080 1 204798177 intergenic variant G/A;C snv 1
rs114190122
CLSTN1
1.000 0.080 1 9819291 intron variant A/G snv 8.6E-03 1
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 1
rs115045402 1.000 0.080 1 152057072 intergenic variant G/A snv 1.7E-02 1
rs115813648
LINC01527
1.000 0.080 1 152949110 3 prime UTR variant T/C snv 1.1E-02 1
rs12083537
IL6R
0.882 0.200 1 154408627 intron variant A/G snv 0.22 1
rs12143327 1.000 0.080 1 112068273 intergenic variant G/A snv 6.7E-02 1
rs12568266 1.000 0.080 1 4133491 intergenic variant G/A;T snv 0.12 1
rs1317209
RNF186
0.925 0.120 1 19813543 upstream gene variant G/A;T snv 0.24 1
rs14271
CLSTN1 ; PIK3CD
1.000 0.080 1 9729092 3 prime UTR variant C/T snv 2.2E-02 1