Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 20
rs1805007
MC1R
0.695 0.280 16 89919709 missense variant C/A;G;T snv 4.4E-02 10
rs6059655
RALY
0.790 0.080 20 34077942 intron variant A/G snv 0.95 10
rs16891982
SLC45A2
0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 9
rs17833789 0.807 0.080 17 57153267 intergenic variant C/A snv 0.37 8
rs9392504 0.827 0.120 6 412802 downstream gene variant G/A snv 0.44 7
rs12913832
HERC2
0.763 0.200 15 28120472 intron variant A/G snv 0.50 7
rs1129038
HERC2
0.851 0.120 15 28111713 3 prime UTR variant C/T snv 0.49 0.50 6
rs1393350
LOC107984363 ; TYR
0.851 0.160 11 89277878 intron variant G/A snv 0.17 5
rs1800407
OCA2
0.807 0.200 15 27985172 missense variant C/T snv 4.7E-02 4.9E-02 5
rs6707137 0.882 0.040 2 88254832 regulatory region variant G/A snv 0.12 4
rs1042602
LOC107984363 ; TYR
0.925 0.080 11 89178528 missense variant C/A snv 0.25 0.24 4
rs4778138
OCA2
0.851 0.080 15 28090674 intron variant A/G;T snv 4
rs4911414 0.882 0.120 20 34141638 regulatory region variant T/G snv 0.73 3
rs12931267
FANCA
1.000 0.040 16 89752324 intron variant C/G snv 4.7E-02 3
rs1667394
HERC2
15 28285036 intron variant C/A;T snv 3
rs864745
JAZF1
0.763 0.320 7 28140937 intron variant T/C snv 0.41 3
rs703978
ZMIZ1
1.000 0.080 10 79184390 intron variant C/G;T snv 0.68 3
rs1015362 0.925 0.080 20 34150806 regulatory region variant C/T snv 0.42 2
rs12185725 1.000 0.080 2 239028127 regulatory region variant A/G snv 0.31 2
rs2671427 1.000 0.080 6 385735 intergenic variant T/C snv 0.57 2
rs62389423 1.000 0.040 6 421281 intergenic variant G/A;T snv 8.5E-02 2
rs258322
CDK10
0.925 0.120 16 89689495 intron variant A/G;T snv 2
rs77733403
DBNDD1
16 90014315 intron variant T/C snv 0.24 2
rs520015
DOCK8
9 211762 upstream gene variant C/G snv 0.54 2