Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10209110 | 1.000 | 0.120 | 2 | 100056230 | intron variant | C/T | snv | 0.47 | 1 | ||
rs11123810 | 0.925 | 0.200 | 2 | 100142823 | intron variant | T/C | snv | 0.37 | 2 | ||
rs11123811 | 1.000 | 0.120 | 2 | 100143710 | intron variant | T/C | snv | 0.55 | 1 | ||
rs6712515 | 0.925 | 0.160 | 2 | 100190052 | intron variant | T/A;C | snv | 3 | |||
rs11676922 | 0.925 | 0.160 | 2 | 100190478 | intron variant | T/A | snv | 0.51 | 4 | ||
rs9653442 | 1.000 | 0.120 | 2 | 100208905 | intron variant | C/T | snv | 0.46 | 2 | ||
rs1160542 | 1.000 | 0.120 | 2 | 100215693 | intron variant | G/A | snv | 0.45 | 1 | ||
rs34619498 | 1.000 | 0.120 | 4 | 100505575 | intron variant | T/C | snv | 2.3E-02 | 1 | ||
rs3775369 | 1.000 | 0.120 | 4 | 100512097 | intron variant | G/A | snv | 3.8E-02 | 1 | ||
rs3783613 | 0.851 | 0.200 | 1 | 100731231 | missense variant | G/A;C | snv | 4.0E-06; 9.9E-03 | 6 | ||
rs16910526 | 0.742 | 0.280 | 12 | 10118488 | stop gained | A/C;G | snv | 6.2E-02 | 12 | ||
rs10275421 | 1.000 | 0.120 | 7 | 101299780 | non coding transcript exon variant | G/A | snv | 7.2E-02 | 1 | ||
rs8029797 | 1.000 | 0.120 | 15 | 101365954 | non coding transcript exon variant | T/A;G | snv | 1 | |||
rs678347 | 1.000 | 0.120 | 8 | 101451374 | intron variant | G/A;C | snv | 1 | |||
rs646514 | 1.000 | 0.120 | 8 | 101453833 | upstream gene variant | C/G;T | snv | 1 | |||
rs17266594 | 0.807 | 0.280 | 4 | 101829765 | intron variant | T/C | snv | 0.25 | 0.27 | 7 | |
rs10516487 | 0.752 | 0.360 | 4 | 101829919 | missense variant | G/A;T | snv | 0.26; 8.0E-06 | 11 | ||
rs3733197 | 0.742 | 0.320 | 4 | 101918130 | missense variant | G/A | snv | 0.31 | 0.30 | 13 | |
rs12434439 | 0.925 | 0.160 | 14 | 102068203 | upstream gene variant | G/C;T | snv | 2 | |||
rs3844283 | 0.882 | 0.200 | 3 | 10222796 | missense variant | C/G | snv | 0.37 | 0.35 | 3 | |
rs708035 | 0.925 | 0.120 | 3 | 10234479 | missense variant | T/A | snv | 0.73 | 0.70 | 2 | |
rs28362491 | 0.592 | 0.720 | 4 | 102500998 | non coding transcript exon variant | ATTG/- | delins | 56 | |||
rs1241312324 | 0.925 | 0.200 | 4 | 102567083 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
rs948138 | 1.000 | 0.120 | 11 | 102630934 | downstream gene variant | G/A | snv | 0.59 | 1 | ||
rs1799969 | 0.637 | 0.560 | 19 | 10284116 | missense variant | G/A | snv | 0.11 | 9.3E-02 | 38 |