Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 187 | ||
rs121434592 | 0.595 | 0.640 | 14 | 104780214 | missense variant | C/T | snv | 4.0E-06 | 54 | ||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 34 | ||
rs121913459 | 0.672 | 0.160 | 9 | 130872896 | missense variant | C/T | snv | 25 | |||
rs156697 | 0.672 | 0.560 | 10 | 104279427 | missense variant | A/G;T | snv | 0.35 | 25 | ||
rs1057519743 | 0.827 | 0.120 | Y | 1196852 | missense variant | A/C | snv | 6 | |||
rs866838052 | 0.851 | 0.160 | 7 | 143267618 | missense variant | C/A | snv | 6 | |||
rs780634396 | 0.882 | 0.120 | 18 | 63318618 | missense variant | T/C | snv | 4.0E-06 | 5 | ||
rs1057519721 | 0.882 | 0.120 | 9 | 5078360 | missense variant | A/G | snv | 4 | |||
rs1057519723 | 0.925 | 0.120 | 9 | 5078362 | missense variant | A/C;G;T | snv | 2 | |||
rs4948488 | 0.925 | 0.120 | 10 | 61925395 | intron variant | C/A;T | snv | 2 | |||
rs529311209 | 0.925 | 0.120 | 22 | 40409754 | missense variant | G/A;C;T | snv | 3.3E-05; 8.2E-06 | 2 | ||
rs1346944271 | 1.000 | 0.120 | 9 | 5090497 | missense variant | G/A | snv | 1.4E-05 | 1 | ||
rs189434316 | 0.925 | 0.120 | 14 | 92231568 | intergenic variant | A/T | snv | 4.1E-02 | 2 | ||
rs35958982 | 1.000 | 0.120 | 13 | 28034336 | missense variant | C/T | snv | 1.3E-02 | 5.0E-02 | 1 | |
rs62527607 | 0.827 | 0.160 | 8 | 103141321 | non coding transcript exon variant | G/T | snv | 0.14 | 5 | ||
rs1800629 | 0.472 | 0.920 | 6 | 31575254 | upstream gene variant | G/A | snv | 0.12 | 0.14 | 169 | |
rs2393732 | 0.925 | 0.120 | 10 | 62007470 | intron variant | G/A | snv | 0.15 | 2 | ||
rs4925 | 0.677 | 0.560 | 10 | 104263031 | missense variant | C/A | snv | 0.25 | 0.23 | 28 | |
rs11980379 | 0.882 | 0.120 | 7 | 50402283 | 3 prime UTR variant | T/C | snv | 0.25 | 3 | ||
rs12430881 | 1.000 | 0.120 | 13 | 28020665 | intron variant | T/C | snv | 0.28 | 1 | ||
rs4958351 | 0.882 | 0.120 | 5 | 153790814 | intron variant | G/A;T | snv | 0.31 | 3 | ||
rs3780135 | 1.000 | 0.120 | 9 | 36840626 | missense variant | G/A | snv | 0.88 | 0.77 | 1 |