Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 12
rs2814778
CADM3-AS1 ; ACKR1
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 11
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs715
CPS1
1.000 0.040 2 210678331 3 prime UTR variant T/C snv 0.28 10
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs150813342
GFI1B
9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs35979828
NFE2
12 54292096 intron variant C/T snv 5.0E-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
rs2954031 8 125479491 intron variant G/T snv 0.42 8
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs9532434
COG6
0.807 0.120 13 39781776 intron variant T/A;C snv 8
rs2228467
CYP8B1 ; KRBOX1 ; ACKR2
1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02 8
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs174549
FADS2 ; FADS1
0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 8
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 8
rs10810657 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 7
rs6782228 3 128604581 intergenic variant G/C snv 0.28 7
rs34599082
ACKR1 ; CADM3-AS1
1 159205704 missense variant C/T snv 1.1E-02 9.9E-03 7
rs3731211
CDKN2A
9 21986848 intron variant T/A snv 0.74 7
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv 7
rs9260620
HLA-A
6 29955314 upstream gene variant T/G snv 0.24 7