Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs57749775 | 0.851 | 0.080 | 12 | 52904822 | missense variant | A/G;T | snv | 1.7E-03; 4.0E-06 | 6 | ||
rs10433937 | 0.882 | 0.080 | 4 | 87308948 | intron variant | T/A;C;G | snv | 4 | |||
rs10020432 | 0.925 | 0.080 | 4 | 73455883 | 3 prime UTR variant | A/G | snv | 0.54 | 2 | ||
rs1140409 | 0.925 | 0.080 | 17 | 64500552 | missense variant | A/C | snv | 5.4E-02 | 5.0E-02 | 2 | |
rs12104272 | 0.925 | 0.080 | 19 | 49644795 | intron variant | G/A | snv | 0.44 | 2 | ||
rs2298839 | 0.925 | 0.080 | 4 | 73445127 | splice region variant | A/G;T | snv | 0.54 | 2 | ||
rs2679757 | 0.925 | 0.080 | 8 | 102858590 | intron variant | A/G | snv | 0.37 | 2 | ||
rs4646038 | 0.925 | 0.080 | 1 | 15506705 | intron variant | C/T | snv | 7.0E-06 | 2 | ||
rs571462252 | 0.925 | 0.080 | 12 | 52904720 | missense variant | G/A | snv | 2 | |||
rs675520 | 0.925 | 0.080 | 6 | 137672095 | non coding transcript exon variant | A/G;T | snv | 2 | |||
rs6834059 | 0.925 | 0.080 | 4 | 73435958 | intron variant | C/G | snv | 0.23 | 2 | ||
rs8021276 | 0.925 | 0.080 | 14 | 92110162 | upstream gene variant | A/G;T | snv | 2 | |||
rs2289030 | 0.882 | 0.120 | 12 | 94834510 | non coding transcript exon variant | G/C | snv | 9.7E-02 | 6.3E-02 | 6 | |
rs16851720 | 0.827 | 0.120 | 3 | 141744456 | intron variant | A/C | snv | 0.21 | 5 | ||
rs843645 | 0.827 | 0.120 | 2 | 54247527 | intron variant | T/A;G | snv | 0.19 | 5 | ||
rs121918664 | 0.851 | 0.120 | 5 | 1254395 | missense variant | C/T | snv | 5.2E-05 | 9.1E-05 | 4 | |
rs10945859 | 0.882 | 0.120 | 6 | 162721570 | intron variant | T/C | snv | 0.17 | 3 | ||
rs1431315635 | 0.882 | 0.120 | 6 | 26092928 | missense variant | C/T | snv | 4.0E-06 | 3 | ||
rs1485766 | 0.882 | 0.120 | 4 | 176689730 | intron variant | T/A;G | snv | 3 | |||
rs376373278 | 0.882 | 0.120 | 17 | 58279015 | missense variant | G/A;C | snv | 4.2E-06 | 3 | ||
rs3844942 | 0.882 | 0.120 | 4 | 189571800 | intergenic variant | T/C | snv | 3 | |||
rs755284374 | 0.882 | 0.120 | 6 | 26093122 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 3 | ||
rs767864210 | 0.882 | 0.120 | 4 | 94657500 | missense variant | G/A;T | snv | 8.0E-05 | 2.1E-05 | 3 | |
rs897206619 | 0.882 | 0.120 | 6 | 26093128 | missense variant | C/T | snv | 3.5E-05 | 3 | ||
rs972427414 | 0.882 | 0.120 | 17 | 58279379 | missense variant | A/G | snv | 3 |