Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs77581414 | 1.000 | 0.080 | 19 | 10823418 | non coding transcript exon variant | T/A;C | snv | 1 | |||
rs1800057 | 0.776 | 0.200 | 11 | 108272729 | missense variant | C/A;G | snv | 1.7E-02 | 11 | ||
rs1801516 | 0.627 | 0.400 | 11 | 108304735 | missense variant | G/A | snv | 0.11 | 0.11 | 39 | |
rs10861905 | 0.925 | 0.120 | 12 | 108373556 | regulatory region variant | C/A | snv | 7.6E-02 | 2 | ||
rs2278911 | 0.925 | 0.080 | 3 | 108579413 | missense variant | C/T | snv | 0.16 | 0.12 | 2 | |
rs2273669 | 0.925 | 0.080 | 6 | 108963986 | intron variant | A/G | snv | 0.19 | 2 | ||
rs3787016 | 0.677 | 0.280 | 19 | 1090804 | intron variant | A/G | snv | 0.78 | 24 | ||
rs1046040 | 0.925 | 0.080 | 19 | 1095515 | upstream gene variant | G/A | snv | 0.21 | 2 | ||
rs768623239 | 0.662 | 0.640 | 1 | 109689278 | missense variant | A/G | snv | 1.5E-05 | 26 | ||
rs75823044 | 1.000 | 0.080 | 13 | 109708437 | intron variant | C/T | snv | 7.6E-03 | 1 | ||
rs7483 | 0.742 | 0.320 | 1 | 109737079 | missense variant | C/T | snv | 4.0E-06; 0.35 | 0.26 | 11 | |
rs11102001 | 0.925 | 0.080 | 1 | 109757069 | missense variant | G/A | snv | 9.4E-02 | 0.16 | 4 | |
rs7986346 | 0.925 | 0.080 | 13 | 109801260 | intron variant | G/A;C;T | snv | 2 | |||
rs3746165 | 0.925 | 0.080 | 19 | 1102212 | upstream gene variant | A/G | snv | 0.54 | 3 | ||
rs2301241 | 0.827 | 0.160 | 9 | 110257228 | upstream gene variant | G/A;T | snv | 5 | |||
rs2536 | 0.776 | 0.240 | 1 | 11106656 | 3 prime UTR variant | T/C | snv | 5.8E-02 | 11 | ||
rs11691517 | 1.000 | 0.080 | 2 | 111135519 | intron variant | T/G | snv | 0.22 | 1 | ||
rs56366063 | 1.000 | 0.080 | 2 | 111146954 | intron variant | C/A | snv | 7.2E-02 | 1 | ||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 92 | ||
rs4938723 | 0.574 | 0.680 | 11 | 111511840 | intron variant | T/C | snv | 0.32 | 60 | ||
rs2788612 | 1.000 | 0.080 | 1 | 111873741 | intron variant | T/C | snv | 0.96 | 1 | ||
rs3806317 | 0.925 | 0.080 | 1 | 11188159 | intron variant | A/G | snv | 3.4E-02 | 2 | ||
rs1034528 | 0.882 | 0.120 | 1 | 11189075 | intron variant | G/C | snv | 0.30 | 5 | ||
rs14133 | 0.807 | 0.200 | 11 | 111911973 | 5 prime UTR variant | G/C | snv | 0.27 | 7 | ||
rs17036508 | 0.925 | 0.080 | 1 | 11195977 | 3 prime UTR variant | T/C | snv | 9.0E-02 | 4 |