Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs116112266 | 2 | 107482651 | intron variant | G/C | snv | 3.5E-03 | 1 | ||||
rs1799852 | 3 | 133756878 | synonymous variant | C/T | snv | 0.13 | 0.11 | 5 | |||
rs8177240 | 3 | 133758857 | intron variant | T/C;G | snv | 0.29 | 5 | ||||
rs6762719 | 3 | 133761973 | non coding transcript exon variant | A/G | snv | 0.31 | 4 | ||||
rs9990333 | 3 | 196100334 | intergenic variant | C/T | snv | 0.42 | 4 | ||||
rs184908836 | 3 | 82041833 | intron variant | A/G | snv | 3.8E-03 | 1 | ||||
rs73214671 | 4 | 7570384 | intron variant | G/A | snv | 1.5E-02 | 1 | ||||
rs150548770 | 5 | 55020802 | intron variant | T/C | snv | 5.4E-03 | 2 | ||||
rs2442120 | 5 | 118970884 | intron variant | A/C | snv | 0.98 | 2 | ||||
rs3797579 | 5 | 75574232 | intron variant | A/G | snv | 9.9E-04 | 1 | ||||
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
rs116009877 | 6 | 25715429 | regulatory region variant | G/A;T | snv | 4 | |||||
rs13191659 | 6 | 27033276 | intron variant | C/G;T | snv | 4 | |||||
rs111722075 | 6 | 25373818 | intron variant | C/T | snv | 0.11 | 2 | ||||
rs113507773 | 6 | 26255511 | upstream gene variant | G/A | snv | 0.10 | 2 | ||||
rs143130997 | 6 | 109780207 | intron variant | G/A | snv | 5.9E-03 | 2 | ||||
rs181143083 | 6 | 157434218 | intron variant | T/A | snv | 7.5E-04 | 2 | ||||
rs202056061 | 6 | 25494109 | intron variant | AGTT/- | delins | 2.8E-02 | 2 | ||||
rs35237909 | 6 | 27256188 | 3 prime UTR variant | ATCT/- | delins | 4.2E-02 | 1 | ||||
rs4642515 | 6 | 32664039 | non coding transcript exon variant | T/A;G | snv | 1 | |||||
rs7385804 | 0.851 | 0.120 | 7 | 100638347 | intron variant | C/A | snv | 0.65 | 14 | ||
rs111991936 | 7 | 23289983 | regulatory region variant | G/A | snv | 1.1E-02 | 1 | ||||
rs10097946 | 8 | 36920273 | intron variant | C/A | snv | 1.0E-02 | 1 | ||||
rs10101752 | 8 | 37125160 | intergenic variant | G/A | snv | 1.2E-02 | 1 |