Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519966 | 0.882 | 0.080 | 17 | 49619064 | missense variant | A/C;T | snv | 3 | |||
rs1057519972 | 0.882 | 0.080 | 17 | 49619327 | missense variant | A/T | snv | 3 | |||
rs1351213477 | 1.000 | 0.080 | 16 | 79211708 | stop gained | C/G;T | snv | 4.0E-06; 1.2E-05 | 3 | ||
rs1057519971 | 1.000 | 0.080 | 17 | 49619326 | missense variant | T/C;G | snv | 2 | |||
rs193920894 | 0.925 | 0.080 | 17 | 49619281 | missense variant | A/C | snv | 2 | |||
rs1057519964 | 1.000 | 0.080 | 17 | 49619282 | missense variant | A/C | snv | 1 | |||
rs1057519965 | 1.000 | 0.080 | 17 | 49619280 | missense variant | G/A;C | snv | 8.0E-06 | 1 | ||
rs1057519967 | 1.000 | 0.080 | 17 | 49619063 | missense variant | A/C;G | snv | 1 | |||
rs193921065 | 1.000 | 0.080 | 17 | 49619062 | missense variant | G/C | snv | 4.0E-06 | 1 | ||
rs1057519968 | 0.925 | 0.120 | 17 | 49619070 | missense variant | A/C;T | snv | 2 | |||
rs1057519969 | 0.925 | 0.120 | 17 | 49619069 | missense variant | C/G | snv | 2 | |||
rs1057519970 | 0.925 | 0.120 | 17 | 49619068 | missense variant | C/A | snv | 2 | |||
rs1057519999 | 0.763 | 0.160 | 17 | 7674247 | missense variant | T/C;G | snv | 12 | |||
rs876660807 | 0.763 | 0.160 | 17 | 7674248 | missense variant | T/C | snv | 12 | |||
rs121913284 | 0.776 | 0.160 | 3 | 179203765 | missense variant | T/A;G | snv | 11 | |||
rs1057519938 | 0.776 | 0.160 | 3 | 179203764 | missense variant | A/C;T | snv | 10 | |||
rs1057519939 | 0.776 | 0.160 | 3 | 179203763 | missense variant | A/C | snv | 10 | |||
rs1057519947 | 0.790 | 0.160 | 19 | 52212730 | missense variant | G/A | snv | 9 | |||
rs1057519962 | 0.827 | 0.160 | 18 | 51067035 | missense variant | G/A;T | snv | 6 | |||
rs776941569 | 0.851 | 0.160 | 8 | 11853378 | frameshift variant | AG/- | del | 1.6E-04 | 1.5E-04 | 6 | |
rs1057519862 | 0.851 | 0.160 | 17 | 39723405 | missense variant | G/A | snv | 5 | |||
rs28931588 | 0.701 | 0.200 | 3 | 41224606 | missense variant | G/A;C;T | snv | 17 | |||
rs1057520009 | 0.790 | 0.200 | 2 | 61492337 | missense variant | C/T | snv | 4.4E-06 | 14 | ||
rs121913228 | 0.742 | 0.200 | 3 | 41224621 | missense variant | T/C;G | snv | 14 | |||
rs1057519940 | 0.752 | 0.200 | 3 | 179218308 | missense variant | G/T | snv | 13 |