Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7744813 | 0.925 | 0.040 | 6 | 72933566 | intron variant | C/A | snv | 0.66 | 3 | ||
rs9318086 | 0.882 | 0.040 | 13 | 23858328 | intron variant | A/G | snv | 0.55 | 3 | ||
rs10089517 | 0.925 | 0.040 | 8 | 59266162 | intergenic variant | C/A | snv | 0.31 | 2 | ||
rs1057518829 | 1.000 | 0.040 | X | 49230343 | stop gained | T/A | snv | 2 | |||
rs1064583 | 0.925 | 0.040 | 6 | 116125413 | missense variant | A/C;G | snv | 0.37 | 2 | ||
rs10860860 | 0.925 | 0.040 | 12 | 102387055 | non coding transcript exon variant | A/T | snv | 0.28 | 2 | ||
rs11873439 | 1.000 | 0.040 | 18 | 69077051 | intergenic variant | A/C | snv | 0.17 | 2 | ||
rs1635529 | 0.925 | 0.040 | 12 | 48001319 | intron variant | T/G | snv | 0.78 | 2 | ||
rs1644731 | 0.925 | 0.040 | 19 | 10021323 | missense variant | T/A;C | snv | 4.0E-06; 0.52 | 2 | ||
rs17122571 | 0.925 | 0.040 | 12 | 48027251 | upstream gene variant | A/G | snv | 8.2E-02 | 2 | ||
rs17400325 | 1.000 | 0.040 | 2 | 177701185 | missense variant | T/C | snv | 3.2E-02 | 2.8E-02 | 2 | |
rs2233789 | 0.925 | 0.040 | 19 | 10013026 | upstream gene variant | C/A;T | snv | 2 | |||
rs2973644 | 0.925 | 0.040 | 5 | 44384081 | intron variant | C/A;T | snv | 2 | |||
rs3026393 | 0.925 | 0.040 | 11 | 31790667 | intron variant | A/C;G;T | snv | 0.48; 8.0E-06; 7.6E-05 | 2 | ||
rs339501 | 0.925 | 0.040 | 5 | 44365531 | intron variant | C/T | snv | 0.94 | 2 | ||
rs3741834 | 0.925 | 0.040 | 12 | 91111607 | upstream gene variant | G/A | snv | 2.6E-02 | 2 | ||
rs3759223 | 0.925 | 0.040 | 12 | 91113006 | upstream gene variant | A/G | snv | 2.7E-02 | 2 | ||
rs669676 | 1.000 | 0.040 | 3 | 99730008 | intron variant | A/G | snv | 0.45 | 2 | ||
rs747797174 | 0.925 | 0.040 | 15 | 74070978 | missense variant | C/A;G;T | snv | 1.2E-05 | 2 | ||
rs79002828 | 0.925 | 0.040 | 5 | 44318015 | intron variant | A/G | snv | 9.6E-03 | 2 | ||
rs9747347 | 1.000 | 0.040 | 17 | 81639794 | intron variant | T/A;C;G | snv | 2 | |||
rs9866391 | 1.000 | 0.040 | 3 | 141357242 | intron variant | T/C | snv | 0.41 | 2 | ||
rs10113215 | 1.000 | 0.040 | 8 | 59219635 | intergenic variant | A/G | snv | 0.33 | 1 | ||
rs10462070 | 1.000 | 0.040 | 5 | 44305647 | intron variant | A/G | snv | 1.2E-02 | 1 | ||
rs10488 | 1.000 | 0.040 | 11 | 102797291 | synonymous variant | C/G;T | snv | 4.0E-06; 5.7E-02 | 1 |