Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519825 | 0.882 | 0.120 | X | 101356176 | missense variant | C/G | snv | 1 | |||
rs1057519826 | 0.882 | 0.120 | X | 101356177 | missense variant | A/T | snv | 1 | |||
rs121434592 | 0.595 | 0.640 | 14 | 104780214 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs1555114766 | 11 | 108317486 | stop gained | G/A | snv | 1 | |||||
rs28904921 | 0.763 | 0.320 | 11 | 108329202 | missense variant | T/G | snv | 4.0E-05 | 6.3E-05 | 7 | |
rs1057519915 | 0.851 | 0.160 | 1 | 11109318 | missense variant | A/C | snv | 5 | |||
rs1057519916 | 0.882 | 0.160 | 1 | 11109320 | missense variant | T/A | snv | 4 | |||
rs1057519913 | 0.925 | 0.120 | 1 | 11157172 | missense variant | G/C | snv | 3 | |||
rs786205165 | 0.882 | 0.120 | 1 | 11157173 | missense variant | C/A;T | snv | 4 | |||
rs1057519914 | 0.851 | 0.240 | 1 | 11157174 | missense variant | A/G | snv | 5 | |||
rs1213469537 | 0.882 | 0.080 | 7 | 116559145 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 1 | |
rs56391007 | 0.752 | 0.200 | 7 | 116771936 | missense variant | C/T | snv | 7.9E-03 | 9.0E-03 | 2 | |
rs1057519854 | 0.882 | 0.080 | 10 | 121488063 | missense variant | A/T | snv | 5 | |||
rs121913476 | 0.851 | 0.080 | 10 | 121498520 | missense variant | A/C;T | snv | 5 | |||
rs1057519045 | 0.851 | 0.160 | 10 | 121498522 | missense variant | T/G | snv | 6 | |||
rs1057519901 | 0.925 | 0.080 | 10 | 121498525 | missense variant | T/G | snv | 5 | |||
rs11249433 | 0.827 | 0.160 | 1 | 121538815 | intron variant | A/C;G | snv | 3 | |||
rs1801725 | 0.633 | 0.600 | 3 | 122284910 | missense variant | G/T | snv | 0.13 | 0.11 | 2 | |
rs1057519943 | 0.790 | 0.160 | 12 | 132676598 | missense variant | G/C;T | snv | 5 | |||
rs1057519944 | 0.882 | 0.160 | 12 | 132676599 | missense variant | G/A | snv | 5 | |||
rs121913348 | 0.763 | 0.480 | 7 | 140781617 | missense variant | C/A;G;T | snv | 16 | |||
rs796065354 | 0.882 | 0.080 | 6 | 151944320 | missense variant | A/G | snv | 1 | |||
rs1057519827 | 6 | 152011697 | missense variant | G/C | snv | 1 | |||||
rs1057519714 | 6 | 152094402 | missense variant | T/C | snv | 1 | |||||
rs1057519715 | 1.000 | 0.080 | 6 | 152098779 | missense variant | T/A | snv | 1 |