Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 4
rs2428494
HLA-B
0.827 0.160 6 31354420 intron variant T/A;C snv 5
rs2544026
HDAC7
0.925 0.080 12 47792780 non coding transcript exon variant T/A snv 0.19 2
rs56389811
HDAC7
1.000 12 47811575 intron variant C/A;T snv 1
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 1
rs4491851
GLB1
0.925 0.080 3 33042493 intron variant G/A snv 0.50 2
rs11255504
GATA3
0.925 0.080 10 8062378 intron variant A/G;T snv 2
rs174621
FADS2
1.000 11 61862632 non coding transcript exon variant G/A;C snv 1
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs28635831
COG6
0.925 0.080 13 39745817 intron variant A/G snv 0.27 2
rs35441874
CLEC16A
0.882 0.120 16 11119164 intron variant T/A snv 0.19 3
rs35032408
CLEC16A
0.925 0.080 16 11121567 intron variant T/C;G snv 2
rs2056625
CD247
0.925 0.080 1 167451062 intron variant G/A snv 0.27 2
rs2056626
CD247
0.882 0.080 1 167451188 intron variant T/G snv 0.30 2
rs58521088
BACH2
0.925 0.080 6 90275479 intron variant A/T snv 0.27 2
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 8
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs117710327 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 5
rs7936312 0.882 0.080 11 76582682 intergenic variant G/T snv 0.44 5
rs10414065 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 4
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 4
rs62322662 0.925 0.080 4 122438414 intergenic variant A/G snv 5.1E-02 4
rs1775554 0.882 0.080 10 9012377 intergenic variant A/C snv 0.35 3
rs4739738 0.882 0.120 8 80379410 intron variant G/A snv 0.60 3