Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1043679457 | 0.752 | 0.400 | 5 | 60927745 | intron variant | C/A;G;T | snv | 33 | |||
rs104894107 | 0.882 | 0.160 | 9 | 69064942 | missense variant | G/C;T | snv | 3.6E-05; 2.8E-05 | 6 | ||
rs104894699 | 0.925 | 0.120 | 19 | 50323694 | missense variant | C/T | snv | 4 | |||
rs1057518011 | 1 | 1535766 | missense variant | C/T | snv | 4 | |||||
rs1057518796 | 1.000 | 6 | 33443751 | frameshift variant | C/- | delins | 3 | ||||
rs1057518821 | 1.000 | 1 | 42930671 | frameshift variant | -/C | delins | 5 | ||||
rs1057518936 | 0.925 | 0.120 | 19 | 7541025 | missense variant | C/G | snv | 3 | |||
rs1057518965 | 0.882 | 0.320 | 11 | 108244812 | frameshift variant | A/- | delins | 5 | |||
rs1057519389 | 0.695 | 0.400 | 10 | 129957324 | missense variant | C/A;G;T | snv | 46 | |||
rs1057519429 | 0.807 | 0.240 | 19 | 13235666 | missense variant | C/G;T | snv | 15 | |||
rs1057520918 | 0.790 | 0.160 | 19 | 13262780 | missense variant | C/T | snv | 11 | |||
rs1064797245 | 0.776 | 0.280 | 19 | 41970540 | missense variant | G/A | snv | 12 | |||
rs1114167423 | 0.882 | 0.240 | 9 | 32984704 | stop gained | T/A | snv | 6 | |||
rs113994095 | 0.701 | 0.360 | 15 | 89327201 | missense variant | C/T | snv | 5.1E-04 | 6.7E-04 | 31 | |
rs113994097 | 0.724 | 0.400 | 15 | 89323426 | missense variant | C/G | snv | 9.7E-04 | 7.9E-04 | 22 | |
rs11538758 | 0.882 | 0.160 | 20 | 4699534 | missense variant | C/A;T | snv | 8 | |||
rs118204095 | 1.000 | 0.160 | 11 | 119091414 | missense variant | G/A;T | snv | 4.5E-05 | 3 | ||
rs118204096 | 1.000 | 0.160 | 11 | 119091432 | missense variant | G/A | snv | 3 | |||
rs119456965 | 1.000 | 0.080 | 5 | 139050960 | stop gained | G/A | snv | 8.0E-06 | 7.0E-06 | 3 | |
rs120074125 | 0.882 | 0.160 | 11 | 6393301 | missense variant | T/G | snv | 4.0E-06 | 7 | ||
rs1208917022 | 1.000 | 0.040 | 12 | 6936663 | missense variant | A/G | snv | 3 | |||
rs121908212 | 0.732 | 0.160 | 19 | 13303877 | missense variant | G/A | snv | 14 | |||
rs121908214 | 0.925 | 0.080 | 19 | 13230185 | missense variant | T/G | snv | 4 | |||
rs121908217 | 0.851 | 0.120 | 19 | 13308452 | missense variant | C/T | snv | 4.0E-06 | 9 | ||
rs121908224 | 1.000 | 0.080 | 19 | 13235262 | missense variant | C/T | snv | 2 |