Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2388334 | 0.882 | 0.040 | 6 | 98143746 | intron variant | A/G | snv | 0.39 | 5 | ||
rs1452075 | 1.000 | 0.040 | 3 | 62495388 | intron variant | C/T | snv | 0.73 | 4 | ||
rs11787216 | 1.000 | 0.040 | 8 | 141605122 | intron variant | C/T | snv | 0.26 | 2 | ||
rs13294439 | 1.000 | 0.040 | 9 | 23358877 | intron variant | A/C | snv | 0.32 | 2 | ||
rs1553518509 | 1.000 | 0.040 | 2 | 148468916 | stop gained | C/T | snv | 2 | |||
rs2898883 | 1.000 | 0.040 | 17 | 49405591 | intron variant | G/A | snv | 0.23 | 2 | ||
rs526126 | 1.000 | 0.040 | 11 | 61857413 | intron variant | G/C;T | snv | 0.81; 8.0E-06 | 2 | ||
rs10497655 | 1.000 | 0.040 | 2 | 184597314 | intron variant | T/C;G | snv | 1 | |||
rs10498676 | 0.925 | 0.040 | 6 | 11026766 | intron variant | G/A | snv | 0.18 | 1 | ||
rs121908445 | 0.925 | 0.040 | 7 | 148147542 | missense variant | T/C | snv | 3.3E-04 | 1.7E-04 | 1 | |
rs1276388879 | 1.000 | 0.040 | 1 | 151405647 | missense variant | A/C;G | snv | 1 | |||
rs1372713010 | 1.000 | 0.040 | 1 | 151428041 | missense variant | G/A | snv | 1 | |||
rs1396313317 | 1.000 | 0.040 | 7 | 147562137 | splice acceptor variant | G/A;C | snv | 4.0E-06 | 1 | ||
rs1418634444 | 1.000 | 0.040 | 1 | 151408777 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
rs1452048149 | 1.000 | 0.040 | 1 | 151404828 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs1476293577 | 1.000 | 0.040 | 1 | 151428188 | missense variant | G/A;C | snv | 1 | |||
rs1484207450 | 1.000 | 0.040 | 1 | 151405155 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
rs1557863430 | 1.000 | 0.040 | 1 | 151405229 | missense variant | T/C | snv | 1 | |||
rs1557863440 | 1.000 | 0.040 | 1 | 151405233 | missense variant | T/C | snv | 1 | |||
rs1557863546 | 1.000 | 0.040 | 1 | 151405263 | missense variant | T/A | snv | 1 | |||
rs1557867853 | 1.000 | 0.040 | 1 | 151406330 | missense variant | G/A | snv | 1 | |||
rs1557870645 | 1.000 | 0.040 | 1 | 151407271 | missense variant | C/T | snv | 1 | |||
rs1557874046 | 1.000 | 0.040 | 1 | 151408807 | missense variant | T/G | snv | 1 | |||
rs1557901347 | 1.000 | 0.040 | 1 | 151424027 | missense variant | G/C | snv | 1 | |||
rs1557902023 | 1.000 | 0.040 | 1 | 151424154 | missense variant | G/C | snv | 1 |