Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10905718 1.000 0.040 10 6072893 upstream gene variant A/G snv 0.25 1
rs13132245 1.000 0.040 4 122128437 intergenic variant A/G snv 0.11 1
rs13140464 0.925 0.040 4 122578590 regulatory region variant G/T snv 0.10 1
rs2836883 0.882 0.080 21 39094818 intergenic variant G/A snv 0.23 1
rs2844559 1.000 0.040 6 31372298 intron variant C/T snv 8.0E-02 1
rs4147359 0.925 0.040 10 6066476 upstream gene variant G/A snv 0.33 1
rs7426056 0.807 0.120 2 203747335 regulatory region variant A/G snv 0.81 1
rs7556897 0.807 0.120 2 227795396 intergenic variant C/G;T snv 1
rs7791854 1.000 0.040 7 77427905 downstream gene variant C/T snv 3.3E-03 1
rs34762726
BSN
1.000 0.040 3 49651777 missense variant G/A snv 0.27 0.28 1
rs1788097
CD226
0.925 0.040 18 69876452 intron variant C/T snv 0.56 1
rs601338
FUT2 ; LOC105447645
0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 1
rs17683107
GAS7
1.000 0.040 17 9921085 intron variant G/A snv 0.13 1
rs3749171
GPR35
0.807 0.120 2 240630275 missense variant C/T snv 0.16; 9.4E-06 0.19 1
rs3134883
IL2RA
1.000 0.040 10 6058762 intron variant G/A snv 0.23 1
rs10883371
LINC01475 ; NKX2-3
1.000 0.040 10 99532698 upstream gene variant C/A snv 0.54 1
rs6971637
LOC101927243
1.000 0.040 7 77425403 non coding transcript exon variant C/T snv 7.1E-03 1
rs415595
LOC105371082 ; RMI2 ; TNP2
1.000 0.040 16 11269835 intron variant A/G snv 0.46 1
rs56258221
LOC105377891
0.925 0.040 6 90320722 intron variant T/C snv 0.13 1
rs4391646
LOC112268276
1.000 0.040 1 166208147 intron variant T/C snv 0.22 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
rs633683
PHLDB1
1.000 0.040 11 118634025 non coding transcript exon variant T/C snv 0.58 1
rs7937682
PPP2R1B ; SIK2
0.925 0.040 11 111709215 intron variant G/A;C snv 1
rs60652743
PRKD2
0.925 0.040 19 46702450 intron variant A/G snv 0.16 1