Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
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
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
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 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
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
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
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 6
rs16903574
OTULINL
0.882 0.120 5 14610200 missense variant C/A;G snv 4.0E-06; 5.6E-02 6
rs5743618
TLR1
0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 6
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 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
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5