Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1360780 | 0.708 | 0.320 | 6 | 35639794 | intron variant | T/A;C | snv | 31 | |||
rs1344706 | 0.701 | 0.160 | 2 | 184913701 | intron variant | A/C;T | snv | 21 | |||
rs1137070 | 0.763 | 0.160 | X | 43744144 | synonymous variant | T/C | snv | 0.62 | 9 | ||
rs686 | 0.807 | 0.080 | 5 | 175441697 | 3 prime UTR variant | G/A;C;T | snv | 9 | |||
rs130058 | 0.790 | 0.120 | 6 | 77463564 | 5 prime UTR variant | T/A;G | snv | 8 | |||
rs900418273 | 0.807 | 0.120 | 11 | 113393764 | missense variant | A/G | snv | 8 | |||
rs1042114 | 0.807 | 0.120 | 1 | 28812463 | missense variant | G/C;T | snv | 0.91 | 6 | ||
rs10196867 | 0.925 | 0.080 | 2 | 79751234 | intron variant | C/G;T | snv | 5 | |||
rs751416416 | 0.882 | 0.120 | 8 | 53250920 | missense variant | C/A;T | snv | 8.3E-06; 4.1E-06 | 5 | ||
rs2910709 | 0.882 | 0.120 | 5 | 37811762 | non coding transcript exon variant | A/G;T | snv | 4 | |||
rs11030096 | 0.925 | 0.160 | 11 | 27643996 | intron variant | T/A;C | snv | 3 | |||
rs265981 | 0.925 | 0.080 | 5 | 175443899 | 5 prime UTR variant | A/G;T | snv | 3 | |||
rs1022563 | 0.925 | 0.080 | 20 | 1973693 | intron variant | C/G;T | snv | 2 | |||
rs1389752 | 0.925 | 0.080 | 9 | 13235288 | intron variant | A/G;T | snv | 2 | |||
rs1530351 | 0.925 | 0.080 | 17 | 65135491 | intron variant | G/A;C | snv | 2 | |||
rs16917234 | 0.925 | 0.080 | 11 | 27676827 | intron variant | T/A;C | snv | 2 | |||
rs6556547 | 0.925 | 0.080 | 5 | 161333168 | intron variant | C/A;T | snv | 2 | |||
rs988712 | 0.925 | 0.160 | 11 | 27541835 | intron variant | G/A;T | snv | 2 | |||
rs1122079 | 1.000 | 0.080 | 17 | 65218385 | intron variant | A/C;T | snv | 1 | |||
rs1714984 | 1.000 | 0.080 | 17 | 12714384 | intron variant | A/G;T | snv | 1 | |||
rs2270162 | 1.000 | 0.080 | 7 | 69596980 | intron variant | C/G;T | snv | 1 | |||
rs2288156 | 1.000 | 0.080 | 17 | 8741536 | missense variant | C/A;T | snv | 4.0E-06; 8.8E-02 | 1 | ||
rs274618 | 1.000 | 0.080 | 7 | 86642700 | upstream gene variant | T/A;C | snv | 1 | |||
rs3219790 | 1.000 | 0.080 | 16 | 10183568 | upstream gene variant | CACACACACACACACACA/-;CA;CACA;CACACA;CACACACA;CACACACACA;CACACACACACA;CACACACACACACA;CACACACACACACACA;CACACACACACACACACACA;CACACACACACACACACACACA;CACACACACACACACACACACACA;CACACACACACACACACACACACACA;CACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACACACACACA | delins | 1 | |||
rs4648319 | 1.000 | 0.080 | 11 | 113443641 | intron variant | G/A;T | snv | 1 |