Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 5
rs13119723
KIAA1109
0.807 0.280 4 122297158 intron variant A/G snv 0.10 5
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 5
rs6840978
IL21-AS1
0.776 0.160 4 122633552 intron variant C/T snv 0.16 3
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 2
rs12369214
RIC8B
0.807 0.120 12 106804833 intron variant G/A snv 0.41 1
rs1452787
TCF4
0.827 0.160 18 55539976 intron variant A/G snv 0.24 1
rs17683107
GAS7
1.000 0.040 17 9921085 intron variant G/A snv 0.13 1
rs1788097
CD226
0.925 0.040 18 69876452 intron variant C/T snv 0.56 1
rs2844559 1.000 0.040 6 31372298 intron variant C/T snv 8.0E-02 1
rs3134883
IL2RA
1.000 0.040 10 6058762 intron variant G/A snv 0.23 1
rs415595
LOC105371082 ; RMI2 ; TNP2
1.000 0.040 16 11269835 intron variant A/G snv 0.46 1
rs4391646
LOC112268276
1.000 0.040 1 166208147 intron variant T/C snv 0.22 1
rs56258221
LOC105377891
0.925 0.040 6 90320722 intron variant T/C snv 0.13 1
rs60652743
PRKD2
0.925 0.040 19 46702450 intron variant A/G snv 0.16 1
rs6678400
LOC112268276
1.000 0.040 1 166208523 intron variant G/T snv 0.22 1
rs6720394
MIR4435-2HG
0.925 0.040 2 111231795 intron variant T/G snv 0.11 1
rs7937682
PPP2R1B ; SIK2
0.925 0.040 11 111709215 intron variant G/A;C snv 1
rs13132245 1.000 0.040 4 122128437 intergenic variant A/G snv 0.11 1
rs2836883 0.882 0.080 21 39094818 intergenic variant G/A snv 0.23 1
rs7556897 0.807 0.120 2 227795396 intergenic variant C/G;T snv 1
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 2
rs13140464 0.925 0.040 4 122578590 regulatory region variant G/T snv 0.10 1
rs7426056 0.807 0.120 2 203747335 regulatory region variant A/G snv 0.81 1