Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35259020 9 134085798 intergenic variant CT/- delins 0.18 3
rs4332427 10 24569461 intergenic variant A/G snv 0.21 3
rs4916483 3 196180782 intergenic variant T/C snv 0.12 3
rs55771711 1.000 0.040 10 131989233 intergenic variant G/C snv 0.24 3
rs5872391 5 154655826 intergenic variant AA/-;A delins 0.35 3
rs6068729 20 53931121 intergenic variant C/T snv 0.19 3
rs609018 12 3962735 regulatory region variant T/A;G snv 3
rs62064595 17 45383008 regulatory region variant A/G snv 9.8E-02 3
rs632057 6 139512875 intron variant T/G snv 0.57 3
rs643381 6 139518286 intron variant C/A;G snv 3
rs6538148 12 88424702 intergenic variant C/G;T snv 3
rs6569992 6 135131014 intergenic variant G/A;C;T snv 3
rs668459 6 139514552 intron variant C/T snv 0.51 3
rs72837788 6 24789643 downstream gene variant G/A snv 2.7E-02 3
rs747844459 6 36634250 regulatory region variant C/G;T snv 3
rs875741 5 173860848 intergenic variant G/A;C snv 3
rs888194 12 109549113 downstream gene variant C/G snv 0.50 3
rs9392465 6 3162144 upstream gene variant C/A snv 0.57 3
rs9483788 6 135114363 intergenic variant T/C snv 0.19 3
rs9850274 3 196195556 downstream gene variant A/G snv 0.76 3
rs10131894 1.000 0.040 14 74980176 regulatory region variant C/G snv 0.49 2
rs1031868 8 97627834 upstream gene variant A/G snv 0.11 2
rs10420951 19 18526808 upstream gene variant C/G snv 0.81 2
rs10849020 12 4222843 intergenic variant C/G snv 0.22 2
rs10910476 1 234599210 regulatory region variant C/A;T snv 2