Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13132430 4 99302913 downstream gene variant G/A;C snv 1
rs13248499 8 120848349 intergenic variant G/A;T snv 1
rs1419980 12 7622296 upstream gene variant A/G snv 0.17 1
rs1457436 14 66378025 intron variant A/G;T snv 3.3E-02 1
rs149963466 1 8173210 regulatory region variant G/A;C;T snv 1
rs1651274 5 158593417 downstream gene variant A/G snv 0.34 1
rs17411031 0.925 0.120 8 19994799 regulatory region variant C/G snv 0.25 1
rs17576323 2 187138391 intron variant T/C snv 0.15 1
rs17799912 19 41029098 upstream gene variant C/T snv 0.18 1
rs189213544 7 80713459 intergenic variant G/A snv 3.4E-04 1
rs1919484 1.000 0.040 8 20012165 intergenic variant G/A snv 0.23 1
rs1942880 18 60125977 intron variant C/T snv 0.37 1
rs1945391 11 122649583 regulatory region variant A/C;T snv 1
rs199607859 6 139514281 intron variant G/T snv 0.39 1
rs2197089 0.925 0.080 8 19968862 downstream gene variant G/A snv 0.61 1
rs2203452 2 226230042 intergenic variant A/G snv 0.66 1
rs2366858 7 80711306 regulatory region variant C/A snv 0.94 1
rs2434612 5 158595033 TF binding site variant A/G snv 0.31 1
rs2534596 7 38238191 downstream gene variant A/G snv 0.32 1
rs255054 16 67983453 upstream gene variant A/C;G snv 1
rs2652834 15 63104668 intron variant A/C;G;T snv 1
rs2764209 6 34729337 intergenic variant T/A snv 0.33 1
rs2878349 1 107006623 intergenic variant G/A snv 0.28 1
rs295849 17 36804493 intergenic variant G/T snv 0.44 1
rs3104435 1 30572662 regulatory region variant A/G snv 0.80 1