Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs56163822 | 1.000 | 0.080 | 12 | 100493323 | 5 prime UTR variant | G/T | snv | 4.7E-02 | 2.8E-02 | 2 | |
rs35724 | 0.925 | 0.040 | 12 | 100561600 | intron variant | C/G | snv | 0.52 | 3 | ||
rs1921 | 1 | 1014228 | missense variant | G/A;C | snv | 0.36 | 1 | ||||
rs104894630 | 0.882 | 0.120 | 17 | 10692805 | missense variant | G/A | snv | 4 | |||
rs587777220 | 0.882 | 0.120 | 17 | 10692932 | missense variant | C/T | snv | 1.2E-05 | 7.0E-06 | 4 | |
rs9514828 | 0.752 | 0.440 | 13 | 108269025 | intron variant | C/T | snv | 0.35 | 12 | ||
rs12583006 | 0.807 | 0.320 | 13 | 108285104 | intron variant | T/A | snv | 0.21 | 8 | ||
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
rs4374383 | 0.776 | 0.200 | 2 | 112013193 | intron variant | A/G | snv | 0.58 | 10 | ||
rs187238 | 0.602 | 0.680 | 11 | 112164265 | intron variant | C/A;G | snv | 48 | |||
rs1946518 | 0.602 | 0.760 | 11 | 112164735 | intron variant | T/G | snv | 0.60 | 46 | ||
rs4849133 | 2 | 112923864 | downstream gene variant | C/A;T | snv | 2 | |||||
rs2070666 | 0.882 | 0.120 | 11 | 116830958 | intron variant | T/A;C | snv | 4 | |||
rs236918 | 0.776 | 0.160 | 11 | 117220893 | non coding transcript exon variant | G/A;C | snv | 10 | |||
rs75961395 | 0.763 | 0.280 | 7 | 117509123 | missense variant | G/A;T | snv | 4.0E-05 | 10 | ||
rs1420111973 | 1.000 | 0.080 | 9 | 117712527 | synonymous variant | T/C | snv | 7.0E-06 | 2 | ||
rs954917585 | 10 | 121479973 | missense variant | G/A | snv | 8.0E-06 | 1.4E-05 | 1 | |||
rs868564661 | 10 | 121487415 | missense variant | G/A | snv | 1 | |||||
rs1061622 | 0.633 | 0.760 | 1 | 12192898 | missense variant | T/G | snv | 0.22 | 0.22 | 33 | |
rs1801282 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 131 | |
rs1805192 | 0.510 | 0.840 | 3 | 12379739 | missense variant | C/G | snv | 121 | |||
rs2243250 | 0.570 | 0.760 | 5 | 132673462 | upstream gene variant | C/T | snv | 0.35 | 61 | ||
rs10833 | 0.776 | 0.160 | 4 | 141733394 | 3 prime UTR variant | T/A;C | snv | 10 | |||
rs121434622 | 1.000 | 0.080 | X | 147936534 | missense variant | T/A | snv | 2 | |||
rs1290547844 | 19 | 15273041 | missense variant | C/T | snv | 4.0E-06 | 1 |