Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1275609 | 12 | 75877403 | intron variant | G/A | snv | 0.40 | 3 | ||||
rs143193096 | 15 | 98916098 | missense variant | G/A;C | snv | 8.4E-05; 4.0E-06 | 3 | ||||
rs151134704 | 4 | 102616435 | splice region variant | C/T | snv | 1.6E-04 | 9.1E-05 | 3 | |||
rs16856823 | 2 | 169343942 | intron variant | A/T | snv | 4.6E-02 | 3 | ||||
rs199592697 | 3 | 13854632 | missense variant | C/T | snv | 1.7E-04 | 1.1E-04 | 3 | |||
rs2290263 | 7 | 25847658 | intergenic variant | G/A | snv | 0.77 | 3 | ||||
rs2453580 | 17 | 19535008 | non coding transcript exon variant | T/C | snv | 0.37 | 3 | ||||
rs2928148 | 15 | 41109352 | intron variant | G/A | snv | 0.44 | 3 | ||||
rs35004449 | 3 | 52818881 | 3 prime UTR variant | G/T | snv | 0.27 | 3 | ||||
rs35716097 | 5 | 177379635 | intron variant | C/T | snv | 0.34 | 3 | ||||
rs36096257 | 2 | 121281207 | missense variant | G/A | snv | 6.8E-03 | 2.9E-03 | 3 | |||
rs3795503 | 1 | 180936558 | synonymous variant | C/T | snv | 0.31 | 0.27 | 3 | |||
rs3850625 | 1 | 201047168 | missense variant | G/A | snv | 0.12 | 8.9E-02 | 3 | |||
rs4690095 | 4 | 3419582 | intron variant | C/G;T | snv | 3 | |||||
rs4715491 | 6 | 54899522 | intron variant | A/G | snv | 0.17 | 3 | ||||
rs549752 | 18 | 79398225 | intron variant | A/G | snv | 0.40 | 3 | ||||
rs6440003 | 3 | 141375367 | intron variant | G/A | snv | 0.54 | 3 | ||||
rs6484504 | 11 | 31403276 | intron variant | T/C | snv | 0.79 | 3 | ||||
rs7012637 | 8 | 9315699 | intron variant | G/A;C | snv | 3 | |||||
rs7024579 | 9 | 136208567 | 3 prime UTR variant | C/A;T | snv | 3 | |||||
rs7766720 | 6 | 106725104 | non coding transcript exon variant | T/C | snv | 0.16 | 3 | ||||
rs10008637 | 4 | 76492991 | intron variant | T/A;C | snv | 0.35 | 2 | ||||
rs10127790 | 1 | 109348511 | intron variant | C/T | snv | 0.63 | 2 | ||||
rs10206899 | 2 | 73673773 | intron variant | T/C;G | snv | 0.21; 3.9E-05 | 2 | ||||
rs10270542 | 7 | 77894452 | intron variant | A/G | snv | 0.43 | 2 |