Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1081105 | 1.000 | 0.080 | 19 | 44909698 | non coding transcript exon variant | A/C | snv | 3.0E-02 | 1 | ||
rs1167428194 | 1.000 | 0.080 | 19 | 44908634 | missense variant | A/C | snv | 1 | |||
rs28931579 | 19 | 44909236 | missense variant | A/C | snv | 9.5E-05 | 6.3E-05 | 1 | |||
rs121918394 | 0.882 | 0.080 | 19 | 44908786 | missense variant | A/C;G | snv | 6.5E-06 | 5 | ||
rs115299243 | 19 | 44907291 | non coding transcript exon variant | A/G | snv | 7.1E-03 | 1 | ||||
rs1275147925 | 1.000 | 0.080 | 19 | 44906613 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
rs28931576 | 19 | 44907894 | missense variant | A/G | snv | 1.2E-05 | 1.4E-05 | 1 | |||
rs397514253 | 1.000 | 0.080 | 19 | 44908531 | splice acceptor variant | A/G | snv | 1 | |||
rs449647 | 0.925 | 0.120 | 19 | 44905307 | upstream gene variant | A/T | snv | 0.21 | 2 | ||
rs1424027593 | 1.000 | 0.080 | 19 | 44908639 | missense variant | C/A | snv | 1 | |||
rs981058595 | 1.000 | 0.080 | 19 | 44908847 | missense variant | C/A | snv | 1 | |||
rs11542029 | 1.000 | 0.080 | 19 | 44907864 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06; 1.2E-05 | 1 | ||
rs11542041 | 0.677 | 0.480 | 19 | 44908690 | missense variant | C/A;T | snv | 2.1E-05 | 23 | ||
rs121918393 | 0.851 | 0.120 | 19 | 44908756 | missense variant | C/A;T | snv | 1.3E-05; 9.0E-05 | 6 | ||
rs11542037 | 1.000 | 0.080 | 19 | 44908657 | missense variant | C/A;T | snv | 5.2E-06 | 1 | ||
rs121918395 | 19 | 44909032 | missense variant | C/A;T | snv | 6.9E-06; 4.2E-05 | 1 | ||||
rs868094551 | 1.000 | 0.080 | 19 | 44908768 | missense variant | C/A;T | snv | 1 | |||
rs267606661 | 0.763 | 0.120 | 19 | 44909101 | missense variant | C/G;T | snv | 3.9E-04; 1.0E-05 | 10 | ||
rs573658040 | 0.790 | 0.200 | 19 | 44908705 | missense variant | C/G;T | snv | 6.3E-06 | 9 | ||
rs440446 | 0.807 | 0.200 | 19 | 44905910 | missense variant | C/G;T | snv | 0.60 | 8 | ||
rs387906567 | 0.882 | 0.200 | 19 | 44908774 | missense variant | C/G;T | snv | 6.3E-06 | 4 | ||
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 47 | |
rs764929617 | 0.776 | 0.200 | 19 | 44907799 | missense variant | C/T | snv | 4.0E-06 | 8 | ||
rs769455 | 0.827 | 0.120 | 19 | 44908783 | missense variant | C/T | snv | 1.4E-03 | 6.9E-03 | 8 | |
rs121918399 | 0.925 | 0.120 | 19 | 44907843 | missense variant | C/T | snv | 8.0E-06 | 2 |