Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 62 | ||
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 34 | |
rs3918226 | 0.925 | 0.080 | 7 | 150993088 | intron variant | C/T | snv | 5.7E-02 | 12 | ||
rs13108218 | 4 | 3442204 | intron variant | A/G;T | snv | 7 | |||||
rs7740107 | 1.000 | 0.080 | 6 | 130053316 | intron variant | T/A;G | snv | 6 | |||
rs1264347 | 1.000 | 0.040 | 6 | 30830920 | upstream gene variant | C/T | snv | 7.9E-02 | 4 | ||
rs34720381 | 1 | 171486183 | intron variant | C/T | snv | 7.3E-02 | 4 | ||||
rs6440003 | 3 | 141375367 | intron variant | G/A | snv | 0.54 | 4 | ||||
rs3795503 | 1 | 180936558 | synonymous variant | C/T | snv | 0.31 | 0.27 | 3 | |||
rs6484504 | 11 | 31403276 | intron variant | T/C | snv | 0.79 | 3 | ||||
rs16930370 | 12 | 3278531 | synonymous variant | T/C | snv | 0.16 | 0.20 | 2 | |||
rs2267373 | 22 | 38204535 | intron variant | C/T | snv | 0.58 | 2 | ||||
rs41284816 | 13 | 50081853 | non coding transcript exon variant | G/C;T | snv | 2 | |||||
rs6544743 | 2 | 44163230 | upstream gene variant | T/A;G | snv | 2 | |||||
rs78444298 | 1 | 184702964 | missense variant | G/A | snv | 1.2E-02 | 1.2E-02 | 2 |