Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17757541 | 0.827 | 0.240 | 18 | 63212453 | intron variant | C/G;T | snv | 7 | |||
rs2509049 | 0.827 | 0.160 | 11 | 119095811 | upstream gene variant | C/A;T | snv | 6 | |||
rs2069812 | 0.851 | 0.240 | 5 | 132544224 | intron variant | A/G | snv | 0.54 | 5 | ||
rs764643047 | 0.851 | 0.120 | 3 | 9750336 | missense variant | C/T | snv | 4.0E-06 | 5 | ||
rs773862672 | 0.882 | 0.280 | 1 | 11247922 | missense variant | G/A;C | snv | 1.2E-05 | 6 | ||
rs78768932 | 0.882 | 0.080 | 12 | 120222977 | missense variant | C/G;T | snv | 5.4E-03 | 5.4E-03 | 6 | |
rs1053023 | 0.882 | 0.120 | 17 | 42313598 | 3 prime UTR variant | T/A;C | snv | 4 | |||
rs9610 | 0.882 | 0.240 | 11 | 118001371 | 3 prime UTR variant | G/A;T | snv | 0.51 | 4 | ||
rs1472503583 | 0.925 | 0.160 | 19 | 1360712 | missense variant | C/T | snv | 4.0E-06 | 4 | ||
rs12566340 | 0.925 | 0.200 | 1 | 113877706 | 3 prime UTR variant | C/A;T | snv | 3 | |||
rs604714 | 0.925 | 0.120 | 11 | 119099986 | intron variant | C/A | snv | 0.31 | 3 | ||
rs6857600 | 0.925 | 0.120 | 4 | 88144923 | intron variant | C/T | snv | 0.28 | 3 | ||
rs2227945 | 1.000 | 0.080 | 17 | 43092113 | missense variant | T/C;G | snv | 2.5E-03 | 1.0E-02 | 2 | |
rs3218674 | 1.000 | 0.120 | 11 | 108244860 | synonymous variant | C/G;T | snv | 1.1E-02 | 1.1E-02 | 2 | |
rs355689 | 1.000 | 0.040 | 4 | 77586643 | intron variant | T/A;C | snv | 2 | |||
rs3811021 | 1.000 | 0.080 | 1 | 113814041 | 3 prime UTR variant | A/G | snv | 0.15 | 2 | ||
rs539846 | 1.000 | 0.120 | 15 | 40105735 | intron variant | G/C;T | snv | 2 |