Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 15
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 10
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 9
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs6894249
IRF1-AS1
0.776 0.160 5 132461855 non coding transcript exon variant A/G snv 0.45 9
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 8
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 6
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs7936323 0.882 0.160 11 76582714 intergenic variant G/A snv 0.44 6
rs12365699 0.882 0.120 11 118872577 regulatory region variant G/A snv 0.12 5
rs1444782 0.851 0.240 10 9016708 intergenic variant G/A snv 0.35 5
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 5
rs10993994
MSMB
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 4
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 4
rs1700159
ACVRL1
1.000 0.040 12 51912002 intron variant C/A;G;T snv 4
rs1811069
YDJC
1.000 0.040 22 21627765 upstream gene variant T/A;G snv 4
rs1870940
ZBTB7B
0.851 0.080 1 155011887 intron variant G/A snv 0.22 4
rs2025758 0.882 0.160 10 8799706 intergenic variant T/C snv 0.41 4
rs2070901
FCER1G
0.882 0.120 1 161215268 non coding transcript exon variant G/T snv 0.32 4