Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs532728316 | 0.882 | 0.080 | 20 | 3230205 | missense variant | C/T | snv | 1.0E-04 | 3.5E-05 | 3 | |
rs767468885 | 0.925 | 0.080 | 6 | 38761702 | missense variant | G/A | snv | 5.5E-06 | 7.0E-06 | 2 | |
rs121909387 | 0.925 | 0.080 | 20 | 3228684 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs121909388 | 0.925 | 0.080 | 20 | 3230258 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 2 | |
rs121909389 | 0.925 | 0.080 | 20 | 3230587 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs121909391 | 0.925 | 0.080 | 20 | 3228260 | missense variant | G/A | snv | 8.0E-06 | 2 | ||
rs121909392 | 0.925 | 0.080 | 20 | 3228259 | missense variant | C/T | snv | 1.2E-05 | 2 | ||
rs1191074716 | 1.000 | 0.080 | 20 | 3231514 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
rs1276051624 | 1.000 | 0.080 | 20 | 3234280 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs1298347142 | 1.000 | 0.080 | 20 | 3231520 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
rs1422526172 | 1.000 | 0.080 | 20 | 3228367 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
rs1465111896 | 1.000 | 0.080 | 20 | 3228630 | missense variant | G/A | snv | 1 | |||
rs1482631297 | 1.000 | 0.080 | 20 | 3234227 | stop gained | C/A;G;T | snv | 4.0E-06; 8.0E-06; 4.0E-06 | 1 | ||
rs200106947 | 1.000 | 0.080 | 20 | 3234786 | missense variant | C/A;T | snv | 1.2E-04; 1.2E-05 | 1 | ||
rs566507872 | 1.000 | 0.080 | 20 | 3233949 | missense variant | G/A;T | snv | 1.2E-05; 1.2E-05 | 1 | ||
rs749826950 | 1.000 | 0.080 | 20 | 3229137 | missense variant | T/C;G | snv | 2.4E-05 | 1 | ||
rs752287261 | 1.000 | 0.080 | 20 | 3234176 | missense variant | C/T | snv | 4.8E-05 | 4.9E-05 | 1 | |
rs757244518 | 1.000 | 0.080 | 20 | 3228395 | missense variant | C/T | snv | 1.2E-05 | 7.0E-06 | 1 | |
rs757553189 | 1.000 | 0.080 | 20 | 3228685 | missense variant | G/A;T | snv | 8.0E-06 | 1 | ||
rs759667344 | 1.000 | 0.080 | 20 | 3233936 | missense variant | G/A | snv | 8.0E-06 | 1 | ||
rs762942751 | 1.000 | 0.080 | 20 | 3233594 | missense variant | G/A | snv | 1.2E-05 | 1.4E-05 | 1 | |
rs766567944 | 1.000 | 0.080 | 20 | 3228537 | missense variant | C/T | snv | 1.2E-05 | 7.0E-06 | 1 | |
rs780171125 | 1.000 | 0.080 | 20 | 3230969 | missense variant | C/G;T | snv | 4.0E-06; 1.2E-05 | 1 | ||
rs797045107 | 1.000 | 0.080 | 20 | 3234173 | frameshift variant | TGGCGAAGC/G | delins | 1 |