Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs429358 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 2 | |
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 1 | |
rs1038582488 | 1.000 | 0.160 | 13 | 51946405 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs1052485948 | 1.000 | 0.160 | 13 | 51949764 | missense variant | A/C;G;T | snv | 4.0E-06; 8.0E-06 | 1 | ||
rs1057517310 | 1.000 | 0.160 | 13 | 51949710 | missense variant | C/A | snv | 1 | |||
rs1057520235 | 1.000 | 0.160 | 13 | 51950277 | missense variant | A/G | snv | 1 | |||
rs1131691741 | 1.000 | 0.160 | 13 | 51937305 | missense variant | T/G | snv | 7.0E-06 | 1 | ||
rs1160679283 | 1.000 | 0.160 | 13 | 51935660 | missense variant | A/G | snv | 4.1E-06 | 1 | ||
rs1169959260 | 1.000 | 0.160 | 13 | 51949681 | missense variant | A/C | snv | 7.0E-06 | 1 | ||
rs1173050016 | 1.000 | 0.160 | 13 | 51964924 | missense variant | A/C | snv | 1 | |||
rs1206016866 | 1.000 | 0.160 | 13 | 51944131 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs1212479289 | 1.000 | 0.160 | 13 | 51960191 | missense variant | G/C;T | snv | 1 | |||
rs1213481140 | 1.000 | 0.160 | 13 | 51941201 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
rs1217463955 | 1.000 | 0.160 | 13 | 51958340 | missense variant | G/C | snv | 4.0E-06 | 1 | ||
rs121907990 | 0.925 | 0.240 | 13 | 51937570 | missense variant | T/A;C | snv | 4.0E-06; 2.2E-04 | 1 | ||
rs121907992 | 1.000 | 0.160 | 13 | 51937583 | missense variant | C/T | snv | 2.8E-05 | 5.6E-05 | 1 | |
rs121907993 | 1.000 | 0.160 | 13 | 51949772 | missense variant | G/A;C;T | snv | 6.0E-05; 2.8E-05; 4.0E-06 | 1 | ||
rs121907994 | 1.000 | 0.160 | 13 | 51950116 | missense variant | G/A | snv | 6.8E-05 | 1.4E-05 | 1 | |
rs121907996 | 1.000 | 0.160 | 13 | 51946438 | missense variant | C/T | snv | 3.6E-05 | 5.6E-05 | 1 | |
rs121907997 | 1.000 | 0.160 | 13 | 51958369 | missense variant | G/A;C | snv | 3.6E-05; 4.0E-06 | 1 | ||
rs121907998 | 1.000 | 0.160 | 13 | 51961849 | missense variant | A/C | snv | 5.2E-04 | 4.0E-04 | 1 | |
rs121908000 | 1.000 | 0.160 | 13 | 51958543 | missense variant | A/G | snv | 4.9E-05 | 1 | ||
rs121908001 | 1.000 | 0.160 | 13 | 51960198 | missense variant | C/T | snv | 1 | |||
rs1230241288 | 1.000 | 0.160 | 13 | 51949765 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
rs1282624946 | 1.000 | 0.160 | 13 | 51970579 | missense variant | C/A | snv | 4.0E-06 | 1 |