Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs138450474 | 1.000 | 0.040 | 19 | 35039140 | missense variant | G/A;C | snv | 2.0E-05 | 1 | ||
rs143166100 | 1.000 | 0.040 | 9 | 128607988 | missense variant | C/G | snv | 5.7E-04 | 5.4E-04 | 1 | |
rs1439688451 | 1.000 | 0.040 | 16 | 9798433 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
rs1441152520 | 1.000 | 0.040 | 9 | 128632218 | missense variant | A/G | snv | 1 | |||
rs145873257 | 1.000 | 0.040 | 16 | 7709117 | missense variant | G/A;T | snv | 1.8E-03 | 1 | ||
rs147896487 | 1.000 | 0.040 | 8 | 18084767 | missense variant | C/G | snv | 1.3E-03 | 1.5E-03 | 1 | |
rs150586939 | 1.000 | 0.040 | 18 | 47156119 | splice region variant | A/G | snv | 4.1E-03 | 1 | ||
rs150821246 | 1.000 | 0.040 | 8 | 132129618 | missense variant | C/T | snv | 3.7E-04 | 3.1E-04 | 1 | |
rs1553138299 | 1.000 | 0.040 | 1 | 43403254 | missense variant | C/G | snv | 1 | |||
rs1553154643 | 1.000 | 0.040 | 1 | 43443774 | missense variant | C/T | snv | 1 | |||
rs1553155982 | 1.000 | 0.040 | 1 | 42928996 | missense variant | T/A | snv | 1 | |||
rs1553574522 | 1.000 | 0.040 | 2 | 165331362 | missense variant | T/C | snv | 1 | |||
rs1554098235 | 1.000 | 0.040 | 5 | 162104026 | missense variant | G/A | snv | 1 | |||
rs1554263366 | 1.000 | 0.040 | 6 | 145686284 | missense variant | T/C | snv | 1 | |||
rs1554626549 | 1.000 | 0.040 | 8 | 132170427 | missense variant | G/A | snv | 1 | |||
rs1554759745 | 1.000 | 0.040 | 9 | 128611792 | missense variant | G/A | snv | 1 | |||
rs1554770659 | 1.000 | 0.040 | 9 | 137163819 | missense variant | T/C | snv | 1 | |||
rs1555437424 | 1.000 | 0.040 | 15 | 92924407 | missense variant | G/A | snv | 1 | |||
rs1555445693 | 1.000 | 0.040 | 15 | 93014832 | missense variant | C/T | snv | 1 | |||
rs1555699052 | 1.000 | 0.040 | 17 | 63710782 | missense variant | C/T | snv | 1 | |||
rs1555790846 | 1.000 | 0.040 | 20 | 8790220 | missense variant | C/T | snv | 1 | |||
rs1555841977 | 1.000 | 0.040 | 21 | 6116503 | missense variant | C/T | snv | 1 | |||
rs180922748 | 1.000 | 0.040 | 2 | 166233432 | missense variant | G/C | snv | 1.2E-03 | 1.7E-03 | 1 | |
rs187334123 | 1.000 | 0.040 | 22 | 31797646 | missense variant | G/A;T | snv | 2.2E-03; 1.6E-05 | 1 | ||
rs191333060 | 1.000 | 0.040 | X | 100296405 | missense variant | G/A;C | snv | 1.3E-03 | 1 |