Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs587777570 | 1.000 | 2 | 148947018 | missense variant | G/A | snv | 4 | ||||
rs1052108705 | 6 | 31165217 | missense variant | C/T | snv | 4.1E-06 | 2.1E-05 | 3 | |||
rs587777186 | 0.925 | 18 | 62146023 | missense variant | A/G;T | snv | 3 | ||||
rs768746587 | 6 | 31165136 | missense variant | C/T | snv | 8.4E-06 | 3 | ||||
rs774753616 | 1.000 | 20 | 45419351 | missense variant | G/A | snv | 1.2E-05 | 1.4E-05 | 3 | ||
rs1206736425 | 1 | 161626229 | missense variant | T/C | snv | 2 | |||||
rs1234344050 | 2 | 188984825 | missense variant | C/G | snv | 4.0E-06 | 2 | ||||
rs1387329667 | 9 | 136500595 | missense variant | G/A | snv | 2 | |||||
rs387906617 | 2 | 207567506 | missense variant | A/G | snv | 2 | |||||
rs756434709 | 9 | 136514670 | missense variant | C/T | snv | 2.0E-05 | 7.0E-06 | 2 | |||
rs764120087 | 22 | 41117439 | missense variant | G/A | snv | 8.0E-06 | 2 | ||||
rs12329305 | 2 | 19353152 | synonymous variant | C/A;T | snv | 1.6E-04; 5.5E-02 | 1 | ||||
rs142322800 | 1 | 161548502 | missense variant | T/C | snv | 1.5E-04 | 5.6E-05 | 1 | |||
rs504849 | 3 | 55488911 | intron variant | T/C;G | snv | 1 | |||||
rs524153 | 3 | 55491957 | upstream gene variant | T/A;G | snv | 1 | |||||
rs757956956 | 19 | 34377533 | missense variant | A/G | snv | 4.0E-06 | 1 | ||||
rs869025322 | 0.925 | 0.040 | 4 | 88521653 | missense variant | A/G | snv | 3 | |||
rs769269532 | 1.000 | 0.040 | 17 | 72124262 | missense variant | A/G | snv | 2.4E-05 | 1.4E-05 | 2 | |
rs121912678 | 0.851 | 0.080 | 2 | 157774114 | missense variant | C/G;T | snv | 8 | |||
rs104893951 | 0.851 | 0.080 | 6 | 1610780 | missense variant | T/A;C | snv | 8.0E-06 | 5 | ||
rs4954218 | 0.925 | 0.080 | 2 | 135045855 | intron variant | G/T | snv | 0.83 | 5 | ||
rs527236031 | 0.882 | 0.080 | 20 | 45424323 | missense variant | C/T | snv | 1.6E-05 | 4.2E-05 | 5 | |
rs587777108 | 0.925 | 0.080 | 11 | 63646550 | missense variant | T/C | snv | 5 | |||
rs756632799 | 0.882 | 0.080 | 20 | 45416579 | stop gained | G/T | snv | 1.6E-05 | 7.0E-06 | 5 | |
rs1554442016 | 0.882 | 0.080 | 7 | 19116972 | missense variant | T/A;C | snv | 4 |