Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs191333060 | 1.000 | 0.040 | X | 100296405 | missense variant | G/A;C | snv | 1.3E-03 | 1 | ||
rs1555790846 | 1.000 | 0.040 | 20 | 8790220 | missense variant | C/T | snv | 1 | |||
rs202170644 | 1.000 | 0.040 | 3 | 64147176 | missense variant | C/G | snv | 4.7E-04 | 6.3E-04 | 1 | |
rs145873257 | 1.000 | 0.040 | 16 | 7709117 | missense variant | G/A;T | snv | 1.8E-03 | 1 | ||
rs372761949 | 1.000 | 0.040 | 16 | 7595618 | missense variant | G/A | snv | 2.5E-05 | 1.4E-05 | 1 | |
rs974157467 | 1.000 | 0.040 | 16 | 7676817 | inframe insertion | GCTGCC/-;GCTGCCGCTGCC | delins | 1 | |||
rs972548690 | 1.000 | 0.040 | 17 | 79094526 | stop gained | G/A;T | snv | 2.9E-05 | 1 | ||
rs114684479 | 1.000 | 0.040 | 7 | 103596518 | missense variant | G/T | snv | 1.6E-03 | 1.4E-03 | 1 | |
rs369993428 | 1.000 | 0.040 | 7 | 103556983 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
rs115035120 | 1.000 | 0.040 | 7 | 103483741 | missense variant | C/T | snv | 8.5E-04 | 2.9E-04 | 1 | |
rs368906199 | 1.000 | 0.040 | 4 | 76213464 | missense variant | C/T | snv | 1.5E-04 | 9.1E-05 | 1 | |
rs199692186 | 1.000 | 0.040 | 2 | 166272748 | missense variant | T/C | snv | 6.3E-04 | 5.5E-04 | 1 | |
rs765818027 | 1.000 | 0.040 | 2 | 166293358 | missense variant | C/T | snv | 4.6E-05 | 2.8E-05 | 1 | |
rs1553574522 | 1.000 | 0.040 | 2 | 165331362 | missense variant | T/C | snv | 1 | |||
rs200138205 | 1.000 | 0.040 | 2 | 165365200 | missense variant | G/A;C | snv | 1.7E-04; 3.2E-05 | 1 | ||
rs180922748 | 1.000 | 0.040 | 2 | 166233432 | missense variant | G/C | snv | 1.2E-03 | 1.7E-03 | 1 | |
rs1555841977 | 1.000 | 0.040 | 21 | 6116503 | missense variant | C/T | snv | 1 | |||
rs1553155982 | 1.000 | 0.040 | 1 | 42928996 | missense variant | T/A | snv | 1 | |||
rs752396911 | 1.000 | 0.040 | 3 | 11025564 | missense variant | G/A;C;T | snv | 4.0E-05; 4.0E-06; 1.6E-05 | 1 | ||
rs202020647 | 1.000 | 0.040 | 1 | 37540752 | missense variant | G/A | snv | 1.8E-04 | 1.3E-04 | 1 | |
rs143166100 | 1.000 | 0.040 | 9 | 128607988 | missense variant | C/G | snv | 5.7E-04 | 5.4E-04 | 1 | |
rs1441152520 | 1.000 | 0.040 | 9 | 128632218 | missense variant | A/G | snv | 1 | |||
rs1554759745 | 1.000 | 0.040 | 9 | 128611792 | missense variant | G/A | snv | 1 | |||
rs569997507 | 1.000 | 0.040 | 9 | 128604371 | missense variant | C/T | snv | 4.0E-05 | 4.2E-05 | 1 | |
rs780658554 | 1.000 | 0.040 | 9 | 128584312 | missense variant | C/T | snv | 3.2E-05 | 3.5E-05 | 1 |