Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 15
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 15
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 10
rs61839660
IL2RA
0.776 0.280 10 6052734 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
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 8
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61 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
rs56062135
SMAD3
0.790 0.200 15 67163292 intron variant C/T snv 0.18 6
rs5743618
TLR1
0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 6
rs12365699 0.882 0.120 11 118872577 regulatory region variant G/A snv 0.12 5
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 5
rs55646091 0.925 0.080 11 76588387 upstream gene variant G/A snv 3.0E-02 5
rs9687958 0.827 0.120 5 40496321 intron variant G/T snv 0.60 5
rs9372120
ATG5
0.851 0.280 6 106219660 intron variant T/G snv 0.16 5
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 5