Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17342717 | 6 | 25821542 | intron variant | C/T | snv | 6.1E-02 | 8 | ||||
rs217181 | 16 | 72080103 | intron variant | C/T | snv | 0.20 | 6 | ||||
rs744653 | 2 | 189514024 | regulatory region variant | C/T | snv | 0.84 | 4 | ||||
rs9302635 | 16 | 72110275 | intron variant | T/C;G | snv | 4 | |||||
rs10064177 | 5 | 4439147 | non coding transcript exon variant | G/A | snv | 0.58 | 2 | ||||
rs113036595 | 13 | 95480065 | intron variant | T/- | del | 0.46 | 2 | ||||
rs145811080 | 10 | 124459913 | upstream gene variant | G/A | snv | 6.7E-03 | 2 | ||||
rs17415853 | 12 | 15777871 | intron variant | T/C | snv | 2.0E-02 | 2 | ||||
rs191752533 | 7 | 16788068 | downstream gene variant | T/G | snv | 3.8E-03 | 2 | ||||
rs411988 | 17 | 58631673 | non coding transcript exon variant | G/A;C | snv | 2 | |||||
rs5743077 | 2 | 189832613 | intron variant | G/A;C | snv | 2 | |||||
rs74450770 | 16 | 66237397 | intergenic variant | T/C | snv | 7.2E-03 | 2 | ||||
rs760719 | 22 | 37064409 | downstream gene variant | C/T | snv | 0.34 | 2 | ||||
rs76858924 | 6 | 26261299 | intergenic variant | C/A;T | snv | 2 | |||||
rs9465627 | 6 | 10233702 | intergenic variant | T/G | snv | 6.5E-03 | 2 | ||||
rs987710 | 1.000 | 0.040 | 22 | 22158022 | intron variant | G/A | snv | 0.61 | 4 | ||
rs5742933 | 0.882 | 0.080 | 2 | 189784590 | 5 prime UTR variant | G/A;C | snv | 5 | |||
rs651007 | 0.851 | 0.160 | 9 | 133278431 | upstream gene variant | T/A;C | snv | 22 | |||
rs855791 | 0.701 | 0.400 | 22 | 37066896 | missense variant | A/G;T | snv | 0.57; 4.0E-06 | 38 | ||
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 |