Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17780256
LOC105371887 ; SLC39A11
0.827 0.120 17 72646784 3 prime UTR variant A/C snv 0.18 6
rs10775412
KSR1
0.827 0.120 17 27542007 intron variant A/C snv 0.30 5
rs1551399
LOC105375746
0.827 0.120 8 125527723 intron variant A/C snv 0.46 5
rs61802846
FCGR2A
0.827 0.120 1 161504083 upstream gene variant A/C snv 8.8E-02 5
rs79390277
TANGO6
1.000 0.040 16 68908687 intron variant A/C snv 3.6E-02 1
rs17102823 0.776 0.080 14 34894698 intergenic variant A/C;G snv 10
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 7
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
rs714830
CDKAL1
0.827 0.120 6 20624151 intron variant A/C;G snv 0.13 5
rs7195296 0.827 0.120 16 11655918 intergenic variant A/C;G snv 5
rs4672505 0.827 0.120 2 62333197 regulatory region variant A/C;G;T snv 5
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 7
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 7
rs35874463
SMAD3
0.827 0.120 15 67165360 missense variant A/G snv 4.0E-02 3.4E-02 7
rs11117431 0.807 0.160 16 85981710 intron variant A/G snv 0.18 6
rs13132308
IL21-AS1
0.807 0.160 4 122629959 intron variant A/G snv 0.10 6
rs13407913
ADCY3
0.827 0.120 2 24874775 intron variant A/G snv 0.54 6
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 6
rs2538470 0.827 0.120 7 148523356 intergenic variant A/G snv 0.61 6
rs2816958
NR5A2
0.827 0.120 1 200132792 intron variant A/G snv 0.84 6
rs4561177
RDX ; ZC3H12C
0.807 0.120 11 110091706 intron variant A/G snv 0.36 6
rs7552167 0.807 0.120 1 24192153 upstream gene variant A/G snv 0.87 6