Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 83 | ||
rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 57 | ||
rs7799039 | 0.649 | 0.560 | 7 | 128238730 | upstream gene variant | G/A;C | snv | 33 | |||
rs3745274 | 0.672 | 0.480 | 19 | 41006936 | missense variant | G/A;T | snv | 4.0E-06; 0.27 | 30 | ||
rs1344706 | 0.701 | 0.160 | 2 | 184913701 | intron variant | A/C;T | snv | 21 | |||
rs1555939456 | 0.851 | 0.200 | X | 20187956 | missense variant | T/C | snv | 21 | |||
rs3730358 | 0.724 | 0.360 | 14 | 104780070 | intron variant | G/A;C | snv | 0.16; 4.0E-03 | 14 | ||
rs6994992 | 0.790 | 0.120 | 8 | 31638065 | upstream gene variant | C/A;T | snv | 13 | |||
rs1800955 | 0.827 | 0.160 | 11 | 636784 | upstream gene variant | T/C;G | snv | 8 | |||
rs143396368 | 0.807 | 0.200 | 9 | 69072623 | missense variant | G/A;C | snv | 3.2E-05; 8.0E-06 | 7 | ||
rs518147 | 0.807 | 0.200 | X | 114584109 | 5 prime UTR variant | C/A;G | snv | 7 | |||
rs778293 | 0.807 | 0.120 | 13 | 105516850 | intergenic variant | C/A;T | snv | 7 | |||
rs35753505 | 0.827 | 0.080 | 8 | 31616625 | intergenic variant | T/A;C | snv | 6 | |||
rs3803300 | 0.827 | 0.120 | 14 | 104803442 | 3 prime UTR variant | T/A;C | snv | 6 | |||
rs4765905 | 0.827 | 0.040 | 12 | 2240418 | intron variant | G/A;C | snv | 6 | |||
rs1039002 | 0.851 | 0.080 | 6 | 165741969 | intron variant | G/A;T | snv | 5 | |||
rs11789399 | 0.882 | 0.040 | 9 | 118597008 | intergenic variant | G/A;C | snv | 5 | |||
rs1555910162 | 0.925 | 0.080 | 22 | 50721469 | frameshift variant | -/C | delins | 5 | |||
rs17693963 | 0.882 | 0.040 | 6 | 27742386 | upstream gene variant | A/C;G | snv | 5 | |||
rs781720548 | 0.882 | 0.040 | 20 | 35652946 | stop gained | C/A | snv | 5 | |||
rs2054399 | 0.925 | 0.040 | 3 | 178623794 | intron variant | G/A;C | snv | 4 | |||
rs2076369 | 0.925 | 0.040 | 22 | 38067645 | non coding transcript exon variant | T/A;G | snv | 3 | |||
rs2619539 | 0.925 | 0.040 | 6 | 15620624 | intron variant | C/A;G | snv | 3 | |||
rs989638 | 0.925 | 0.040 | X | 123239256 | intron variant | C/G;T | snv | 3 |