Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10821944
ARID5B
1.000 0.120 10 62025330 3 prime UTR variant G/T snv 0.66 1
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs10892279 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 3
rs10919563
PTPRC
0.925 0.120 1 198731313 intron variant G/A snv 0.21 1
rs10946213 1.000 0.120 6 167102607 intron variant C/T snv 0.35 1
rs10947233
PPT2-EGFL8 ; PPT2
0.925 0.160 6 32156647 intron variant G/C;T snv 3.4E-02 4
rs10947260
TSBP1-AS1 ; BTNL2
1.000 0.120 6 32405408 intron variant T/C snv 0.11 0.11 1
rs10947261
BTNL2 ; TSBP1-AS1
0.882 0.240 6 32405455 splice region variant G/T snv 0.11 4
rs10947434
IP6K3
1.000 0.120 6 33723724 intron variant G/T snv 0.40 1
rs10985070
PHF19
1.000 0.120 9 120873843 intron variant C/A snv 0.47 1
rs10985073
PHF19
1.000 0.120 9 120881577 intron variant T/C snv 0.44 1
rs11051970 1.000 0.120 12 32384554 downstream gene variant G/T snv 0.33 1
rs1105586
ENOX1
1.000 0.120 13 43658497 intron variant T/C snv 0.35 1
rs1105856
ENOX1
1.000 0.120 13 43652931 intron variant G/T snv 0.52 1
rs11066188
HECTD4
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06 4
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 4
rs11089637 1.000 0.120 22 21624807 downstream gene variant T/C snv 0.28 2
rs1111695
PHTF1
1.000 0.120 1 113701277 intron variant C/A snv 0.65 1
rs11121380
SPSB1
1.000 0.120 1 9348900 intron variant A/C snv 0.11 1
rs11148643 1.000 0.120 13 64317065 intergenic variant T/A;C snv 0.46 1
rs111988552
TSPAN5
1.000 0.120 4 98557163 intron variant A/T snv 1
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 5
rs11203366
PADI4
0.925 0.200 1 17331039 missense variant G/A snv 0.56 0.55 1
rs11203368
PADI4
0.925 0.200 1 17340013 intron variant C/T snv 0.57 1
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5