Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10012947 1.000 0.040 4 30491805 regulatory region variant C/T snv 0.33 1
rs1001684 1.000 0.040 5 40810324 intergenic variant C/A snv 0.29 1
rs10077591 1.000 0.040 5 165935005 intergenic variant C/T snv 0.44 1
rs10135277 1.000 0.040 14 35354025 TF binding site variant C/T snv 0.43 1
rs10204454 1.000 0.040 2 193481559 intergenic variant C/T snv 0.44 1
rs10204933 1.000 0.040 2 228206898 intergenic variant A/G snv 0.15 1
rs1021487 1.000 0.040 4 58590920 intergenic variant T/C snv 0.15 1
rs1033023 1.000 0.040 1 239045834 intergenic variant T/A snv 0.36 1
rs10429924 1.000 0.040 1 244227262 intergenic variant C/T snv 8.8E-02 1
rs10498146 1.000 0.040 2 222987318 intergenic variant A/G snv 6.2E-02 1
rs10509852 1.000 0.040 10 107815336 intron variant C/A;T snv 1
rs1075195 1.000 0.040 20 38718108 intergenic variant T/C snv 0.76 1
rs10789369 1.000 0.040 1 73359226 downstream gene variant A/G;T snv 1
rs10829461 1.000 0.040 10 128646955 intergenic variant G/A snv 0.14 1
rs10878577 1.000 0.040 12 67200061 intergenic variant A/C snv 0.64 1
rs10894294 1.000 0.040 11 130960853 intergenic variant C/A;G snv 1
rs10894308 1.000 0.040 11 131022000 intergenic variant G/A;C snv 1
rs10895475 1.000 0.040 11 103593113 intergenic variant C/A;T snv 1
rs10940346 1.000 0.040 5 50510208 intergenic variant G/A snv 0.44 1
rs10967505 1.000 0.040 9 26737658 intergenic variant G/A snv 8.5E-02 1
rs10970384 1.000 0.040 9 3158247 intergenic variant A/C snv 0.21 1
rs10976131 1.000 0.040 9 7226519 intergenic variant T/C snv 0.18 1
rs11027827 1.000 0.040 11 24353633 intergenic variant T/C snv 0.38 1
rs11027857 1.000 0.040 11 24382074 intergenic variant G/A snv 0.51 1
rs1108252 1.000 0.040 2 232688857 intergenic variant T/C snv 0.19 1