Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 1
rs10088247
CSMD1
1.000 0.040 8 3826677 intron variant C/T snv 0.76 1
rs1008953 1.000 0.040 20 45352086 upstream gene variant T/C snv 0.79 1
rs10405308 1.000 0.040 19 1312729 intergenic variant G/A snv 7.9E-02 1
rs1047781
LOC105447645 ; FUT2
0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 1
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 8
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 2
rs1056198
RNF114
0.925 0.040 20 49939692 intron variant C/T snv 0.34 1
rs1062470
PSORS1C1 ; CDSN
0.925 0.040 6 31116658 synonymous variant G/A snv 0.37 0.41 4
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs10782001
FBXL19
1.000 0.040 16 30931304 intron variant G/A snv 0.53 2
rs10852936
ZPBP2
0.925 0.120 17 39875461 intron variant C/T snv 0.39 0.40 2
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 3
rs10889676
IL23R
0.827 0.120 1 67256884 intron variant C/A;T snv 1
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs10979182
LOC105376214
1.000 0.040 9 108054739 regulatory region variant A/G snv 0.44 1
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 3
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 1
rs11121129
LINC01714
1.000 0.040 1 8208035 intron variant G/A snv 0.26 1
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 2
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 1
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs11230563
LOC105369326 ; CD6
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 1