Source: UNIPROT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs192732174 | 0.827 | 0.160 | 3 | 33068245 | missense variant | G/A;T | snv | 4.0E-05; 3.6E-05 | 3 | ||
rs376710410 | 0.827 | 0.160 | 3 | 33065551 | missense variant | A/C | snv | 2.7E-05 | 5.6E-05 | 2 | |
rs72555358 | 0.851 | 0.160 | 3 | 33072644 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 2 | |
rs72555360 | 0.807 | 0.280 | 3 | 33058221 | missense variant | G/A | snv | 4.4E-05 | 6.3E-05 | 2 | |
rs745386663 | 0.807 | 0.160 | 3 | 33051956 | missense variant | G/A | snv | 8.0E-06 | 2.1E-05 | 2 | |
rs72555367 | 0.851 | 0.160 | 3 | 33018482 | missense variant | C/T | snv | 2 | |||
rs1214295886 | 1.000 | 0.120 | 3 | 33052000 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
rs1553610553 | 0.851 | 0.160 | 3 | 33053518 | missense variant | C/G | snv | 1 | |||
rs371582179 | 0.827 | 0.280 | 3 | 33014057 | missense variant | T/C | snv | 3.6E-05 | 6.3E-05 | 1 | |
rs376663785 | 0.827 | 0.160 | 3 | 33051989 | missense variant | A/C | snv | 1.6E-05 | 7.0E-06 | 1 | |
rs72555361 | 0.851 | 0.160 | 3 | 33051766 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
rs72555366 | 0.827 | 0.160 | 3 | 33058200 | missense variant | G/A | snv | 4.4E-05 | 1.2E-04 | 1 | |
rs72555368 | 0.827 | 0.160 | 3 | 33014292 | missense variant | T/C | snv | 1.2E-05 | 1 | ||
rs72555390 | 0.807 | 0.160 | 3 | 33072637 | missense variant | A/G;T | snv | 1 | |||
rs72555392 | 0.807 | 0.200 | 3 | 33072613 | missense variant | C/T | snv | 3.6E-05 | 1 | ||
rs72555393 | 0.851 | 0.160 | 3 | 33072544 | missense variant | G/A | snv | 5.2E-05 | 1.4E-05 | 1 | |
rs749980306 | 0.827 | 0.160 | 3 | 33046150 | missense variant | C/A;G | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs28934886 | 0.882 | 0.160 | 3 | 33016818 | missense variant | C/T | snv | 1.2E-05 | 1 | ||
rs780724173 | 0.851 | 0.160 | 3 | 33018474 | missense variant | C/T | snv | 1.2E-05 | 2.1E-05 | 1 |