Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1228276529 | 1.000 | 0.080 | 1 | 209612203 | missense variant | G/A | snv | 1 | |||
rs1158962067 | 1.000 | 0.080 | 14 | 102975693 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
rs1490814436 | 1.000 | 0.080 | 2 | 201835740 | missense variant | A/T | snv | 1.2E-05 | 1 | ||
rs121913473 | 1.000 | 0.080 | 8 | 38428420 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
rs762093504 | 1.000 | 0.080 | 6 | 2692787 | missense variant | C/A;T | snv | 4.0E-06; 1.6E-05 | 1 | ||
rs746466314 | 1.000 | 0.080 | 11 | 64361697 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs1428512439 | 1.000 | 0.080 | 1 | 45457754 | missense variant | C/G;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
rs1040254222 | 1.000 | 0.080 | 15 | 50611215 | missense variant | T/A;C | snv | 4.0E-06; 8.0E-06 | 1 | ||
rs1336054298 | 1.000 | 0.080 | 2 | 178590298 | missense variant | A/G | snv | 1.4E-05 | 1 | ||
rs576644663 | 1.000 | 0.080 | 2 | 178770479 | missense variant | G/A;C | snv | 4.0E-06; 8.0E-06 | 1 |