Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6921438 | 0.776 | 0.360 | 6 | 43957870 | intergenic variant | G/A;C | snv | 10 | |||
rs6993770 | 0.925 | 0.080 | 8 | 105569300 | intron variant | A/T | snv | 0.31 | 9 | ||
rs10738760 | 0.807 | 0.320 | 9 | 2691186 | regulatory region variant | A/G | snv | 0.56 | 7 | ||
rs4416670 | 0.827 | 0.240 | 6 | 43982716 | intergenic variant | T/C | snv | 0.45 | 7 | ||
rs10761731 | 10 | 63267850 | intron variant | A/T | snv | 0.38 | 6 | ||||
rs114694170 | 1.000 | 0.040 | 5 | 88884379 | non coding transcript exon variant | T/C | snv | 3.6E-02 | 5 | ||
rs10761741 | 1.000 | 0.040 | 10 | 63306426 | intron variant | G/T | snv | 0.38 | 4 | ||
rs2375980 | 9 | 2692622 | intergenic variant | C/G | snv | 0.51 | 3 | ||||
rs4782371 | 1.000 | 0.040 | 16 | 88502423 | intron variant | T/A;G | snv | 3 | |||
rs1740073 | 1.000 | 0.040 | 6 | 43979661 | regulatory region variant | T/C | snv | 0.67 | 2 | ||
rs2375981 | 1.000 | 0.040 | 9 | 2692583 | regulatory region variant | C/G;T | snv | 2 | |||
rs6479877 | 10 | 63118358 | intergenic variant | C/A;G;T | snv | 2 | |||||
rs7767396 | 6 | 43959313 | intergenic variant | A/G | snv | 0.48 | 2 | ||||
rs12199215 | 6 | 44059177 | non coding transcript exon variant | C/T | snv | 0.25 | 2 | ||||
rs7043199 | 1.000 | 0.040 | 9 | 2621145 | intron variant | T/A | snv | 0.18 | 2 | ||
rs2639990 | 1.000 | 0.040 | 18 | 75203596 | intron variant | T/C | snv | 0.12 | 2 | ||
rs10122587 | 9 | 2691951 | intergenic variant | C/G;T | snv | 1 | |||||
rs10967470 | 9 | 2675698 | intergenic variant | A/G | snv | 0.21 | 1 | ||||
rs10967492 | 9 | 2681175 | intergenic variant | T/A | snv | 0.18 | 1 | ||||
rs12214617 | 6 | 43972186 | intergenic variant | G/T | snv | 0.53 | 1 | ||||
rs143479231 | 3 | 193393005 | intergenic variant | G/A | snv | 1.5E-02 | 1 | ||||
rs1776717 | 6 | 43983599 | regulatory region variant | G/A;C | snv | 1 | |||||
rs34528081 | 6 | 43736680 | intron variant | -/T | ins | 0.49 | 1 | ||||
rs4513773 | 6 | 43957789 | intergenic variant | A/G | snv | 0.44 | 1 | ||||
rs6475920 | 9 | 2673933 | intergenic variant | C/A;G | snv | 1 |