Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1114167415 | 0.925 | 0.120 | 7 | 94426514 | missense variant | G/A;C | snv | 2 | |||
rs121912905 | 0.925 | 0.120 | 7 | 94408806 | missense variant | G/T | snv | 2 | |||
rs121912907 | 0.925 | 0.120 | 7 | 94415263 | missense variant | G/T | snv | 2 | |||
rs121912911 | 0.925 | 0.200 | 7 | 94426442 | missense variant | G/C | snv | 2 | |||
rs1554200371 | 0.925 | 0.120 | 6 | 81750332 | missense variant | T/C | snv | 2 | |||
rs66523073 | 0.925 | 0.120 | 17 | 50188777 | missense variant | C/T | snv | 2 | |||
rs67368147 | 0.925 | 0.120 | 17 | 50191805 | missense variant | C/A;T | snv | 2 | |||
rs67445413 | 0.925 | 0.120 | 17 | 50189876 | missense variant | C/A;T | snv | 2 | |||
rs72651645 | 0.925 | 0.160 | 17 | 50191463 | missense variant | C/T | snv | 2 | |||
rs72653178 | 0.925 | 0.120 | 17 | 50188619 | missense variant | C/T | snv | 2 | |||
rs72654795 | 0.925 | 0.120 | 17 | 50188565 | missense variant | C/T | snv | 2 | |||
rs72659304 | 0.925 | 0.120 | 7 | 94425118 | missense variant | G/A | snv | 2 | |||
rs72667031 | 0.925 | 0.120 | 17 | 50197983 | missense variant | C/A | snv | 2 | |||
rs1114167388 | 1.000 | 0.120 | 17 | 50191840 | missense variant | C/G | snv | 1 | |||
rs1114167412 | 1.000 | 0.120 | 7 | 94410492 | missense variant | G/C | snv | 1 | |||
rs1131692320 | 1.000 | 0.120 | 17 | 50187103 | missense variant | C/T | snv | 1 | |||
rs1554396283 | 1.000 | 0.120 | 7 | 94410926 | missense variant | G/T | snv | 1 | |||
rs1800250 | 1.000 | 0.120 | 7 | 94427801 | missense variant | A/C | snv | 1 | |||
rs267606742 | 1.000 | 0.120 | 7 | 94427628 | missense variant | G/A | snv | 1 | |||
rs67609234 | 1.000 | 0.120 | 7 | 94425832 | missense variant | G/A;T | snv | 1 | |||
rs67641695 | 1.000 | 0.120 | 17 | 50188592 | missense variant | C/T | snv | 1 | |||
rs67729041 | 1.000 | 0.120 | 7 | 94409778 | missense variant | G/A;T | snv | 1 | |||
rs72645320 | 1.000 | 0.120 | 17 | 50197053 | missense variant | C/T | snv | 1 | |||
rs72645363 | 1.000 | 0.120 | 17 | 50195931 | missense variant | C/G | snv | 1 | |||
rs72656320 | 1.000 | 0.120 | 17 | 50187095 | missense variant | C/T | snv | 1 |