Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1021001 | 1.000 | 0.080 | 5 | 180777104 | intergenic variant | G/C;T | snv | 1 | |||
rs10521296 | 1.000 | 0.080 | 16 | 53529332 | intergenic variant | G/A | snv | 0.15 | 1 | ||
rs10783050 | 1.000 | 0.080 | 1 | 96571527 | intergenic variant | T/C | snv | 0.28 | 1 | ||
rs10919774 | 1.000 | 0.080 | 1 | 199938588 | intergenic variant | A/G | snv | 5.2E-02 | 1 | ||
rs11205591 | 1.000 | 0.080 | 1 | 39035577 | downstream gene variant | C/G;T | snv | 1 | |||
rs11639988 | 1.000 | 0.080 | 16 | 19933041 | intergenic variant | A/G | snv | 0.16 | 1 | ||
rs11647470 | 1.000 | 0.080 | 16 | 55157878 | intergenic variant | C/T | snv | 0.93 | 1 | ||
rs11664883 | 1.000 | 0.080 | 18 | 60210567 | intergenic variant | T/A | snv | 0.20 | 1 | ||
rs11665563 | 1.000 | 0.080 | 18 | 60208801 | intergenic variant | C/T | snv | 0.20 | 1 | ||
rs11673900 | 1.000 | 0.080 | 2 | 118118540 | intergenic variant | G/A;T | snv | 1 | |||
rs12186500 | 1.000 | 0.080 | 5 | 180749005 | intergenic variant | A/G | snv | 0.41 | 1 | ||
rs1294908 | 1.000 | 0.080 | 7 | 45195521 | intergenic variant | C/T | snv | 0.78 | 1 | ||
rs12964203 | 1.000 | 0.080 | 18 | 60236371 | intergenic variant | T/C | snv | 0.20 | 1 | ||
rs12966550 | 1.000 | 0.080 | 18 | 60244097 | intergenic variant | A/G | snv | 0.20 | 1 | ||
rs12996547 | 1.000 | 0.080 | 2 | 602036 | intergenic variant | C/T | snv | 0.38 | 1 | ||
rs13278851 | 1.000 | 0.080 | 8 | 9893362 | intergenic variant | G/A | snv | 8.6E-02 | 1 | ||
rs1424233 | 1.000 | 0.080 | 16 | 79648854 | regulatory region variant | T/C | snv | 0.44 | 1 | ||
rs1573949 | 1.000 | 0.080 | 3 | 128478439 | downstream gene variant | C/T | snv | 0.70 | 1 | ||
rs17126232 | 1.000 | 0.080 | 8 | 18120141 | intron variant | C/T | snv | 0.11 | 1 | ||
rs17175643 | 1.000 | 0.080 | 18 | 60229509 | intergenic variant | C/A;T | snv | 1 | |||
rs1729408 | 1.000 | 0.080 | 11 | 116804102 | intergenic variant | A/G | snv | 0.48 | 1 | ||
rs17697518 | 1.000 | 0.080 | 18 | 41185695 | intergenic variant | C/T | snv | 9.3E-02 | 1 | ||
rs180096 | 1.000 | 0.080 | 17 | 69946593 | intergenic variant | A/G | snv | 0.75 | 1 | ||
rs1879523 | 1.000 | 0.080 | 2 | 651599 | intergenic variant | A/T | snv | 0.33 | 1 | ||
rs1943226 | 1.000 | 0.080 | 18 | 60367971 | intron variant | T/G | snv | 6.7E-02 | 1 |