Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1465788
ZFP36L1
0.925 0.160 14 68796882 upstream gene variant T/C snv 0.70 2
rs927292
ZFP36L1
1.000 0.120 14 68792124 intron variant C/G snv 0.68 1
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 4
rs11258747
PRKCQ
1.000 0.120 10 6430929 missense variant G/C;T snv 4.0E-06; 0.17 1
rs2269241
PGM1
1.000 0.120 1 63643100 intron variant T/C snv 0.23 2
rs947474
LINC02649 ; LINC02656
0.827 0.440 10 6348488 intron variant G/A snv 0.79 3
rs12251307 1.000 0.120 10 6081532 intergenic variant C/T snv 0.18 1
rs7090530 0.851 0.160 10 6068912 downstream gene variant C/A snv 0.59 1
rs10795791 0.925 0.200 10 6066377 upstream gene variant A/G snv 0.40 1
rs3118470
IL2RA
0.752 0.360 10 6059750 intron variant T/A;C snv 2
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 2
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 4
rs12722495
IL2RA
0.851 0.200 10 6055320 intron variant T/C snv 7.0E-02 1
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 1
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 1
rs1678542
KIF5A
0.790 0.320 12 57574932 intron variant C/G snv 0.42 3
rs2066808
STAT2
0.807 0.280 12 56344189 intron variant A/G snv 0.21 2
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 1
rs2292239
ERBB3
0.742 0.480 12 56088396 intron variant T/G snv 0.65 4
rs11171739
ERBB3
0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49 2
rs705704
RPS26 ; LOC105369780
0.882 0.240 12 56041628 non coding transcript exon variant G/A snv 0.26 1
rs1701704
LOC105369781 ; IKZF4
0.851 0.200 12 56018703 intron variant T/G snv 0.25 5
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10