Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs1063192 | 0.695 | 0.520 | 9 | 22003368 | 3 prime UTR variant | G/A;T | snv | 24 | |||
rs2165241 | 0.716 | 0.360 | 15 | 73929861 | intron variant | T/C | snv | 0.60 | 15 | ||
rs3825942 | 0.716 | 0.320 | 15 | 73927241 | missense variant | G/A;C;T | snv | 0.18; 4.5E-06 | 15 | ||
rs74315329 | 0.732 | 0.240 | 1 | 171636338 | stop gained | G/A | snv | 1.1E-03 | 8.7E-04 | 15 | |
rs11258194 | 0.776 | 0.160 | 10 | 13110400 | missense variant | T/A | snv | 4.4E-02 | 6.0E-02 | 9 | |
rs10120688 | 0.807 | 0.080 | 9 | 22056500 | intron variant | G/A | snv | 0.50 | 7 | ||
rs7049105 | 0.807 | 0.120 | 9 | 22028802 | intron variant | A/G | snv | 0.58 | 7 | ||
rs199746824 | 0.807 | 0.040 | 1 | 171652139 | missense variant | C/G;T | snv | 4.0E-06; 1.6E-05 | 6 | ||
rs10483727 | 0.851 | 0.040 | 14 | 60606157 | upstream gene variant | T/C | snv | 0.45 | 4 | ||
rs4236601 | 0.882 | 0.040 | 7 | 116522675 | upstream gene variant | G/A | snv | 0.28 | 4 | ||
rs1052990 | 0.882 | 0.040 | 7 | 116508316 | 3 prime UTR variant | T/C;G | snv | 3 | |||
rs1333037 | 0.925 | 0.040 | 9 | 22040766 | intron variant | C/T | snv | 0.71 | 3 | ||
rs7037117 | 0.882 | 0.040 | 9 | 117721385 | 3 prime UTR variant | A/G | snv | 0.40 | 3 | ||
rs284491 | 0.925 | 0.040 | 8 | 104946405 | intron variant | C/T | snv | 0.45 | 2 |