Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 6
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 4
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4
rs2596480 0.925 0.120 6 31458208 intron variant C/G;T snv 3
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 2
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 2
rs12540874
GRB10
0.882 0.280 7 50597225 intron variant A/C;G snv 2
rs2205960
TNFSF4
0.763 0.400 1 173222336 intergenic variant G/A;T snv 2
rs7601754
STAT4
0.882 0.160 2 191075725 intron variant G/A;T snv 2
rs7774954
HLA-DQB2
0.925 0.120 6 32756412 3 prime UTR variant C/A;T snv 5.9E-02 2
rs9275245 0.925 0.160 6 32693166 intergenic variant A/G;T snv 2
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 1
rs11171747
ESYT1 ; ZC3H10
1.000 0.040 12 56124624 3 prime UTR variant T/A;G snv 1
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 1
rs2409781
BLK
0.925 0.120 8 11502048 intron variant T/A;C snv 1
rs3130573
PSORS1C2 ; PSORS1C1
1.000 0.040 6 31138491 non coding transcript exon variant A/C;G snv 8.1E-06; 0.33 1
rs35677470
DNASE1L3
0.807 0.160 3 58197909 missense variant G/A;C snv 4.8E-02; 4.0E-06 1
rs35705950 0.763 0.240 11 1219991 splice region variant G/A;T snv 1
rs540386
TRAF6
0.851 0.200 11 36503743 intron variant C/G;T snv 1
rs564732150
MUC22
1.000 0.040 6 31028355 missense variant C/T snv 1
rs58721818 0.851 0.160 6 137922602 regulatory region variant C/G;T snv 1
rs624988 0.925 0.120 1 116721168 regulatory region variant T/A;C snv 1
rs6793295
LRRC34
0.827 0.240 3 169800667 missense variant T/C;G snv 0.37; 1.8E-04 1
rs6832151 0.925 0.160 4 40301616 intergenic variant G/A;T snv 1
rs7190018
ITGAM
1.000 0.040 16 31290157 intron variant G/A;C snv 1