Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17749 | 1.000 | 0.040 | 6 | 38676020 | 3 prime UTR variant | C/T | snv | 1 | |||
rs1345354331 | 1.000 | 0.040 | 3 | 49358221 | missense variant | A/C;T | snv | 6.8E-06; 6.8E-06 | 1 | ||
rs643788 | 1.000 | 0.040 | 11 | 119097048 | missense variant | T/C | snv | 0.42 | 0.38 | 1 | |
rs3093739 | 1.000 | 0.040 | 13 | 108215053 | intron variant | A/G | snv | 8.8E-02 | 1 | ||
rs749124997 | 1.000 | 0.040 | 12 | 102402539 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs770617145 | 1.000 | 0.040 | 17 | 49512716 | missense variant | G/A | snv | 3.4E-05 | 1 | ||
rs10764901 | 1.000 | 0.040 | 10 | 129716598 | intron variant | A/G | snv | 0.62 | 1 | ||
rs11706832 | 1.000 | 0.040 | 3 | 66452557 | intron variant | A/C;G | snv | 1 | |||
rs4598633 | 1.000 | 0.040 | 11 | 96278187 | intron variant | T/A;C | snv | 1 | |||
rs485842 | 1.000 | 0.040 | 11 | 96290050 | intron variant | C/T | snv | 0.26 | 1 | ||
rs7938889 | 1.000 | 0.040 | 11 | 96231355 | intron variant | C/T | snv | 0.48 | 1 | ||
rs1339499 | 1.000 | 0.040 | 9 | 125644174 | intron variant | T/C | snv | 0.29 | 1 | ||
rs473426 | 1.000 | 0.040 | 9 | 125644709 | intron variant | G/C | snv | 0.44 | 1 | ||
rs1982266 | 1.000 | 0.040 | 10 | 52770876 | intron variant | A/G;T | snv | 1 | |||
rs17138945 | 1.000 | 0.040 | 7 | 116703812 | intron variant | T/G | snv | 7.3E-02 | 1 | ||
rs7727115 | 1.000 | 0.040 | 5 | 160474732 | intron variant | G/T | snv | 0.17 | 1 | ||
rs2961920 | 1.000 | 0.040 | 5 | 160484499 | intron variant | C/A | snv | 0.70 | 1 | ||
rs11730 | 1.000 | 0.040 | 2 | 151270497 | 3 prime UTR variant | A/G | snv | 0.36 | 1 | ||
rs2194492 | 1.000 | 0.040 | 2 | 151289680 | 5 prime UTR variant | G/C | snv | 0.53 | 1 | ||
rs2278089 | 1.000 | 0.040 | 2 | 151290158 | upstream gene variant | G/T | snv | 0.69 | 1 | ||
rs3854012 | 1.000 | 0.040 | 2 | 151280592 | intron variant | C/T | snv | 0.44 | 1 | ||
rs6734376 | 1.000 | 0.040 | 2 | 151288153 | intron variant | T/C | snv | 0.27 | 1 | ||
rs372951639 | 1.000 | 0.040 | 16 | 69718484 | missense variant | A/T | snv | 1.6E-05 | 3.5E-05 | 1 | |
rs4253079 | 1.000 | 0.040 | 10 | 49514779 | intron variant | T/G | snv | 8.2E-02 | 1 | ||
rs11603023 | 0.925 | 0.120 | 11 | 118615352 | intron variant | T/C | snv | 0.57 | 1 |