Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11632488 1.000 0.040 15 79975159 upstream gene variant A/G snv 0.20 1
rs13140464 0.925 0.040 4 122578590 regulatory region variant G/T snv 0.10 1
rs2856674 0.925 0.160 6 32691868 regulatory region variant A/G snv 9.8E-02 1
rs4147359 0.925 0.040 10 6066476 upstream gene variant G/A snv 0.33 1
rs74856421 1.000 0.040 16 3723109 downstream gene variant C/T snv 5.6E-02 1
rs1788097
CD226
0.925 0.040 18 69876452 intron variant C/T snv 0.56 1
rs725613
CLEC16A
0.851 0.240 16 11075826 intron variant T/G snv 0.42 1
rs36023390
FOXP1
1.000 0.040 3 71473942 intron variant C/T snv 0.36 1
rs80060485
FOXP1
1.000 0.040 3 71104739 intron variant T/C snv 5.5E-02 1
rs850526
GNGT2 ; ABI3
1.000 0.040 17 49208404 intron variant T/C snv 0.31 1
rs61861422
INPP5A
1.000 0.040 10 132544853 intron variant C/G;T snv 1
rs17649817
KCNIP1
1.000 0.040 5 170529575 intron variant C/A snv 0.11 1
rs1532244
LINC01967
1.000 0.040 3 28016414 intron variant A/G snv 0.17 1
rs56258221
LOC105377891
0.925 0.040 6 90320722 intron variant T/C snv 0.13 1
rs6720394
MIR4435-2HG
0.925 0.040 2 111231795 intron variant T/G snv 0.11 1
rs72837826
MIR4435-2HG
1.000 0.040 2 111175424 intron variant G/T snv 7.8E-02 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
rs145832854
SGSM1
1.000 0.040 22 24914162 intron variant G/A snv 3.1E-02 1
rs79390277
TANGO6
1.000 0.040 16 68908687 intron variant A/C snv 3.6E-02 1
rs4143332
ZDHHC20P2
1.000 0.040 6 31380588 non coding transcript exon variant G/A snv 8.2E-02 1
rs853974 0.882 0.120 6 126747838 intron variant T/C snv 0.77 2
rs4293777
CLNK
0.925 0.080 4 10715315 intergenic variant G/A;C snv 2
rs7731017
DCTN4
0.925 0.080 5 150732056 intron variant T/C snv 8.3E-03 2
rs228614
MANBA
0.925 0.120 4 102657480 intron variant G/A snv 0.50 2