Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 1
rs4112788 0.851 0.120 1 152578800 downstream gene variant A/G;T snv 1
rs4649203 0.851 0.160 1 24193430 intergenic variant G/A snv 0.61 1
rs4676406 0.827 0.120 2 240639691 intergenic variant G/T snv 0.53 1
rs4722404 0.851 0.120 7 3089155 intron variant T/C snv 0.40 1
rs4845454 0.925 0.040 1 152619708 downstream gene variant C/A;T snv 1
rs559928 0.827 0.120 11 64382898 intergenic variant T/C snv 0.77 1
rs6426833 0.827 0.120 1 19845367 TF binding site variant G/A snv 0.52 1
rs6677595 1.000 0.040 1 152617711 downstream gene variant C/G;T snv 1
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 1
rs7426056 0.807 0.120 2 203747335 regulatory region variant A/G snv 0.81 1
rs7552167 0.807 0.120 1 24192153 upstream gene variant A/G snv 0.87 1
rs7556897 0.807 0.120 2 227795396 intergenic variant C/G;T snv 1
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 1
rs8016947 0.925 0.080 14 35363460 intron variant T/G snv 0.60 1
rs9687958 0.827 0.120 5 40496321 intron variant G/T snv 0.60 1
rs999556 0.925 0.080 5 151094113 upstream gene variant A/G snv 0.38 1
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17 2
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 1
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 3
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 1