Source: GWASCAT ×
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 7
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 6
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs17849502
NCF2 ; SMG7
0.827 0.240 1 183563445 missense variant G/A;C;T snv 4.0E-06; 4.0E-06; 3.4E-02 5
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5
rs35677470
DNASE1L3
0.807 0.160 3 58197909 missense variant G/A;C snv 4.8E-02; 4.0E-06 5
rs35929052 0.827 0.160 16 85960878 downstream gene variant C/G;T snv 5
rs6793295
LRRC34
0.827 0.240 3 169800667 missense variant T/C;G snv 0.37; 1.8E-04 5
rs4958880
TNIP1
0.851 0.160 5 151058916 intron variant C/A;G snv 4
rs5754467
CCDC116 ; YDJC
0.851 0.160 22 21630805 upstream gene variant A/G;T snv 4
rs58721818 0.851 0.160 6 137922602 regulatory region variant C/G;T snv 4
rs960709
TNIP1
0.882 0.120 5 151081488 intron variant A/G;T snv 4
rs77583790
IL12A-AS1
0.882 0.080 3 159976265 intron variant G/A;C snv 3
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 3
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 2
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 2
rs4554699 0.925 0.040 1 161638578 intergenic variant A/G snv 2
rs7601754
STAT4
0.882 0.160 2 191075725 intron variant G/A;T snv 2
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 1
rs1059702
IRAK1
0.807 0.280 X 154018741 missense variant A/G snv 0.72 1
rs11117420
LINC02132
1.000 0.040 16 85938316 intron variant G/C;T snv 1
rs11171747
ESYT1 ; ZC3H10
1.000 0.040 12 56124624 3 prime UTR variant T/A;G snv 1
rs11217020
DDX6
1.000 0.040 11 118768644 intron variant G/A;C snv 1
rs1130866
SFTPB
0.827 0.160 2 85666618 missense variant G/A;C snv 0.50 1
rs12540874
GRB10
0.882 0.280 7 50597225 intron variant A/C;G snv 1