Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs386833981 | 0.925 | 0.120 | 13 | 77000517 | missense variant | T/G | snv | 3 | |||
rs104894385 | 0.925 | 0.120 | 13 | 76992176 | stop gained | G/A;T | snv | 2.7E-05; 3.1E-05 | 2 | ||
rs104894386 | 0.925 | 0.120 | 13 | 76995077 | missense variant | G/A;C | snv | 8.0E-06 | 2 | ||
rs1555274338 | 1.000 | 0.120 | 13 | 77000567 | stop gained | G/A;C | snv | 2 | |||
rs28940280 | 0.925 | 0.120 | 13 | 77000580 | missense variant | G/A | snv | 8.0E-06 | 2 | ||
rs386833975 | 0.925 | 0.120 | 13 | 76995990 | missense variant | A/G | snv | 2 | |||
rs386833980 | 0.925 | 0.120 | 13 | 76996086 | stop gained | G/A | snv | 1.6E-05 | 3.5E-05 | 2 | |
rs546989392 | 0.925 | 0.120 | 13 | 76996010 | stop gained | C/T | snv | 2.0E-05 | 7.7E-05 | 2 | |
rs121908292 | 1.000 | 0.120 | 13 | 77000799 | stop gained | G/T | snv | 1 | |||
rs147065248 | 1.000 | 0.120 | 13 | 76996034 | missense variant | T/C | snv | 1.2E-05 | 7.0E-06 | 1 | |
rs148862100 | 1.000 | 0.120 | 13 | 77000866 | missense variant | A/G | snv | 1.3E-05 | 7.0E-06 | 1 | |
rs1555274014 | 1.000 | 0.120 | 13 | 76996128 | splice donor variant | G/A | snv | 1 | |||
rs1566219136 | 1.000 | 0.120 | 13 | 76995993 | missense variant | G/A | snv | 1 | |||
rs200348035 | 1.000 | 0.120 | 13 | 76992182 | stop gained | G/A;T | snv | 4.5E-06 | 1 | ||
rs202146713 | 1.000 | 0.120 | 13 | 76995233 | splice region variant | G/C | snv | 1.2E-05 | 2.1E-05 | 1 | |
rs267606738 | 1.000 | 0.120 | 13 | 76995119 | missense variant | G/A | snv | 1 | |||
rs386833963 | 1.000 | 0.120 | 13 | 77000771 | stop gained | C/A | snv | 1 | |||
rs386833968 | 1.000 | 0.120 | 13 | 77000882 | stop gained | G/A;T | snv | 4.3E-06 | 1 | ||
rs386833971 | 1.000 | 0.120 | 13 | 76995175 | stop gained | C/T | snv | 2.4E-05 | 1 | ||
rs386833972 | 1.000 | 0.120 | 13 | 76995939 | stop gained | T/G | snv | 4.0E-06; 4.0E-06 | 1 | ||
rs386833974 | 1.000 | 0.120 | 13 | 76995980 | stop gained | C/T | snv | 1 | |||
rs386833976 | 1.000 | 0.120 | 13 | 76996008 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
rs386833977 | 1.000 | 0.120 | 13 | 76996028 | missense variant | C/T | snv | 1 | |||
rs386833978 | 1.000 | 0.120 | 13 | 76996035 | missense variant | G/C | snv | 1 | |||
rs730882146 | 1.000 | 0.120 | 13 | 77000680 | missense variant | G/A | snv | 4.0E-06 | 1 |