Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11254413 | 0.851 | 0.120 | 10 | 17162188 | missense variant | G/A | snv | 0.41 | 0.44 | 4 | |
rs207454 | 0.851 | 0.120 | 2 | 31344766 | intron variant | T/G | snv | 0.11 | 0.16 | 4 | |
rs2494752 | 0.790 | 0.120 | 14 | 104797271 | upstream gene variant | A/G | snv | 0.85 | 10 | ||
rs2736109 | 0.851 | 0.120 | 5 | 1296644 | upstream gene variant | C/T | snv | 0.32 | 4 | ||
rs2808668 | 0.851 | 0.120 | 9 | 97690153 | intron variant | C/G;T | snv | 7 | |||
rs353639 | 0.851 | 0.120 | 11 | 35162817 | intron variant | T/G | snv | 0.32 | 5 | ||
rs752681512 | 0.851 | 0.120 | 5 | 7897088 | missense variant | A/G | snv | 2.0E-05 | 4 | ||
rs753535070 | 0.851 | 0.120 | 1 | 155187350 | missense variant | T/C | snv | 8.0E-06 | 5 | ||
rs7972 | 0.851 | 0.120 | 14 | 77326894 | missense variant | G/A | snv | 7.0E-02 | 7.0E-02 | 4 | |
rs80358829 | 0.827 | 0.120 | 13 | 32340327 | missense variant | C/T | snv | 6 | |||
rs1562430 | 0.807 | 0.160 | 8 | 127375606 | intron variant | T/C | snv | 0.41 | 6 | ||
rs2240688 | 0.790 | 0.160 | 4 | 15968726 | 3 prime UTR variant | T/G | snv | 0.22 | 7 | ||
rs5277 | 0.790 | 0.160 | 1 | 186679065 | synonymous variant | C/G;T | snv | 0.12; 8.0E-06 | 9 | ||
rs828907 | 0.827 | 0.160 | 2 | 216108009 | intron variant | G/T | snv | 0.37 | 6 | ||
rs113593938 | 0.790 | 0.200 | 21 | 44250907 | missense variant | C/T | snv | 3.5E-03 | 7 | ||
rs1801200 | 0.790 | 0.200 | 17 | 39723335 | missense variant | A/G;T | snv | 7 | |||
rs2293303 | 0.827 | 0.200 | 3 | 41239336 | synonymous variant | C/T | snv | 3.2E-02 | 1.2E-02 | 7 | |
rs3747093 | 0.732 | 0.200 | 22 | 21630090 | upstream gene variant | G/A | snv | 0.32 | 16 | ||
rs6498486 | 0.776 | 0.200 | 16 | 13919809 | upstream gene variant | A/C | snv | 0.27 | 8 | ||
rs6713088 | 0.763 | 0.200 | 2 | 54118332 | intron variant | C/G | snv | 0.48 | 9 | ||
rs6917 | 0.790 | 0.200 | 17 | 49404181 | 3 prime UTR variant | G/A | snv | 0.16 | 7 | ||
rs1047972 | 0.716 | 0.240 | 20 | 56386407 | missense variant | T/C | snv | 0.85 | 0.84 | 19 | |
rs10511729 | 0.742 | 0.240 | 9 | 23557229 | intron variant | T/G | snv | 0.35 | 11 | ||
rs10811474 | 0.742 | 0.240 | 9 | 21114238 | intergenic variant | A/G | snv | 0.44 | 11 | ||
rs12683422 | 0.742 | 0.240 | 9 | 27969442 | intron variant | C/T | snv | 5.7E-02 | 11 |