Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs137854600 | 0.807 | 0.120 | 3 | 38551504 | missense variant | C/A;T | snv | 6 | |||
rs199473225 | 0.851 | 0.120 | 3 | 38560397 | missense variant | G/A;C | snv | 6 | |||
rs137854606 | 0.882 | 0.120 | 3 | 38604062 | missense variant | C/A | snv | 4 | |||
rs137854612 | 0.851 | 0.120 | 3 | 38560170 | missense variant | C/T | snv | 4 | |||
rs137854615 | 0.851 | 0.120 | 3 | 38550989 | missense variant | A/G | snv | 4 | |||
rs199473229 | 0.882 | 0.120 | 3 | 38560361 | missense variant | A/G | snv | 4 | |||
rs199473244 | 0.851 | 0.120 | 3 | 38557251 | missense variant | C/A | snv | 4 | |||
rs199473556 | 0.851 | 0.120 | 3 | 38630342 | missense variant | G/A | snv | 4 | |||
rs199473092 | 0.925 | 0.080 | 3 | 38608175 | missense variant | A/C | snv | 3 | |||
rs199473096 | 0.882 | 0.120 | 3 | 38606751 | missense variant | G/A | snv | 3 | |||
rs199473103 | 0.925 | 0.120 | 3 | 38606102 | missense variant | A/G | snv | 3 | |||
rs199473143 | 0.925 | 0.080 | 3 | 38597949 | missense variant | T/G | snv | 3 | |||
rs199473207 | 0.882 | 0.120 | 3 | 38566555 | missense variant | G/A | snv | 3 | |||
rs199473051 | 0.925 | 0.120 | 3 | 38633058 | missense variant | C/T | snv | 2 | |||
rs199473070 | 0.925 | 0.120 | 3 | 38613811 | missense variant | A/G;T | snv | 2 | |||
rs199473079 | 1.000 | 0.080 | 3 | 38609860 | missense variant | G/T | snv | 2 | |||
rs199473093 | 0.925 | 0.080 | 3 | 38606802 | missense variant | G/A | snv | 2 | |||
rs199473168 | 0.925 | 0.080 | 3 | 38585846 | missense variant | G/A | snv | 2 | |||
rs199473169 | 0.925 | 0.080 | 3 | 38585821 | missense variant | T/G | snv | 2 | |||
rs199473240 | 0.925 | 0.080 | 3 | 38560176 | missense variant | C/T | snv | 2 | |||
rs199473245 | 0.925 | 0.080 | 3 | 38557236 | missense variant | T/C | snv | 2 | |||
rs199473248 | 0.925 | 0.080 | 3 | 38556565 | missense variant | G/A | snv | 2 | |||
rs199473292 | 0.925 | 0.080 | 3 | 38551391 | missense variant | C/G;T | snv | 2 | |||
rs199473305 | 0.925 | 0.080 | 3 | 38551145 | missense variant | C/T | snv | 1.4E-05 | 2 | ||
rs199473322 | 0.925 | 0.080 | 3 | 38550823 | missense variant | C/G | snv | 2 |