Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 7 | ||
rs10211550 | 1.000 | 0.040 | 2 | 197518575 | intron variant | G/T | snv | 0.37 | 2 | ||
rs1024582 | 1.000 | 0.040 | 12 | 2293080 | intron variant | A/G;T | snv | 2 | |||
rs10503253 | 0.851 | 0.040 | 8 | 4323322 | intron variant | C/A | snv | 0.18 | 5 | ||
rs10520163 | 1.000 | 0.040 | 4 | 169705401 | intron variant | T/A;C | snv | 2 | |||
rs10791097 | 1.000 | 0.040 | 11 | 130848735 | intron variant | T/G | snv | 0.60 | 2 | ||
rs10994359 | 0.827 | 0.040 | 10 | 60462349 | intron variant | T/C | snv | 8.0E-02 | 5 | ||
rs10994397 | 0.851 | 0.040 | 10 | 60519366 | intron variant | C/T | snv | 9.5E-02 | 5 | ||
rs11152369 | 0.851 | 0.040 | 18 | 55399097 | intron variant | A/C | snv | 6.3E-02 | 5 | ||
rs11191419 | 1.000 | 0.040 | 10 | 102852578 | intron variant | T/A | snv | 0.36 | 2 | ||
rs11191454 | 0.776 | 0.160 | 10 | 102900247 | intron variant | A/G | snv | 7.9E-02 | 5 | ||
rs11191580 | 0.827 | 0.040 | 10 | 103146454 | intron variant | T/C | snv | 7.9E-02 | 12 | ||
rs11191582 | 1.000 | 0.040 | 10 | 103153896 | intron variant | G/A | snv | 7.7E-02 | 2 | ||
rs112209031 | 1.000 | 0.040 | 6 | 32524630 | intron variant | T/C;G | snv | 2 | |||
rs113397282 | 1.000 | 0.040 | 6 | 32520273 | intron variant | T/C;G | snv | 2 | |||
rs114086406 | 1.000 | 0.040 | 6 | 32374760 | intron variant | G/A | snv | 2 | |||
rs114274203 | 1.000 | 0.040 | 6 | 31300843 | intron variant | C/T | snv | 2 | |||
rs114277634 | 1.000 | 0.040 | 6 | 31474954 | intron variant | T/A;C | snv | 2 | |||
rs114455101 | 1.000 | 0.040 | 6 | 32465853 | intron variant | T/G | snv | 2 | |||
rs114838832 | 1.000 | 0.040 | 6 | 30937536 | intron variant | A/G | snv | 2 | |||
rs114875775 | 1.000 | 0.040 | 6 | 32521255 | intron variant | A/T | snv | 1.8E-02 | 2 | ||
rs114963521 | 1.000 | 0.040 | 6 | 30791080 | intron variant | C/T | snv | 2 | |||
rs115035678 | 1.000 | 0.040 | 6 | 32381780 | intron variant | A/T | snv | 2 | |||
rs115052633 | 1.000 | 0.040 | 6 | 31621487 | intron variant | C/G;T | snv | 2 | |||
rs115123779 | 1.000 | 0.040 | 6 | 29510044 | intron variant | G/A;C;T | snv | 2 |