Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1041536 | 1.000 | 0.040 | 20 | 9907627 | intergenic variant | T/C | snv | 0.46 | 1 | ||
rs112961612 | 1.000 | 0.040 | 20 | 41872026 | intergenic variant | T/A | snv | 8.2E-02 | 1 | ||
rs113793030 | 1.000 | 0.040 | 10 | 70287104 | upstream gene variant | T/C | snv | 1.7E-02 | 1 | ||
rs115700680 | 1.000 | 0.040 | 1 | 171381070 | intergenic variant | T/G | snv | 1.9E-02 | 1 | ||
rs116065238 | 1.000 | 0.040 | 1 | 171482283 | upstream gene variant | A/G | snv | 4.3E-03 | 1 | ||
rs116237496 | 1.000 | 0.040 | 8 | 101033687 | upstream gene variant | T/C | snv | 4.0E-02 | 1 | ||
rs117070989 | 1.000 | 0.040 | 6 | 137490510 | downstream gene variant | C/A | snv | 8.3E-03 | 1 | ||
rs117129097 | 1.000 | 0.040 | 12 | 128054737 | intron variant | C/G;T | snv | 1.9E-03 | 1 | ||
rs117224174 | 1.000 | 0.040 | 6 | 114654261 | intergenic variant | G/A | snv | 2.2E-02 | 1 | ||
rs12230170 | 1.000 | 0.040 | 12 | 128762838 | intergenic variant | T/A;G | snv | 1 | |||
rs12435940 | 1.000 | 0.040 | 14 | 25552779 | intergenic variant | A/G | snv | 0.97 | 1 | ||
rs12468965 | 1.000 | 0.040 | 2 | 53528621 | downstream gene variant | G/A | snv | 1.8E-02 | 1 | ||
rs138901640 | 1.000 | 0.040 | 9 | 118031487 | intron variant | A/G | snv | 5.5E-03 | 1 | ||
rs139660738 | 1.000 | 0.040 | 12 | 94791412 | intergenic variant | T/C | snv | 6.3E-03 | 1 | ||
rs141480664 | 1.000 | 0.040 | 7 | 4469958 | regulatory region variant | G/A | snv | 1.0E-02 | 1 | ||
rs142609537 | 1.000 | 0.040 | 15 | 95675665 | intron variant | A/G | snv | 1.8E-02 | 1 | ||
rs146594485 | 1.000 | 0.040 | 20 | 3776090 | downstream gene variant | G/A | snv | 6.1E-03 | 1 | ||
rs149969998 | 1.000 | 0.040 | 17 | 13692262 | intergenic variant | G/C;T | snv | 1 | |||
rs150418526 | 1.000 | 0.040 | 17 | 38697587 | upstream gene variant | C/G;T | snv | 1 | |||
rs150616616 | 1.000 | 0.040 | 5 | 121366663 | downstream gene variant | C/G;T | snv | 1 | |||
rs150759334 | 1.000 | 0.040 | 4 | 60800528 | downstream gene variant | T/C | snv | 9.4E-03 | 1 | ||
rs150828104 | 1.000 | 0.040 | 12 | 116337891 | regulatory region variant | TTTTGTTTTG/-;TTTTG;TTTTGTTTTGTTTTG;TTTTGTTTTGTTTTGTTTTG | delins | 1 | |||
rs150934526 | 1.000 | 0.040 | 5 | 121330628 | intron variant | T/C | snv | 1.1E-02 | 1 | ||
rs183819925 | 1.000 | 0.040 | 4 | 175138126 | intron variant | G/T | snv | 9.7E-03 | 1 | ||
rs184148048 | 1.000 | 0.040 | 2 | 66212157 | intergenic variant | A/T | snv | 1.3E-02 | 1 |