Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs761937143 | 1.000 | 0.040 | 18 | 51047229 | synonymous variant | A/C | snv | 8.0E-06 | 1 | ||
rs2230054 | 0.925 | 0.080 | 2 | 218135587 | synonymous variant | C/T | snv | 0.48 | 0.54 | 2 | |
rs1194919682 | 0.925 | 0.040 | 2 | 136115158 | missense variant | A/G | snv | 2 | |||
rs7731017 | 0.925 | 0.080 | 5 | 150732056 | intron variant | T/C | snv | 8.3E-03 | 2 | ||
rs1003723 | 0.925 | 0.080 | 19 | 11113505 | non coding transcript exon variant | C/A;T | snv | 4.0E-06; 0.40 | 2 | ||
rs2076310 | 0.925 | 0.080 | 6 | 33198257 | intron variant | A/G | snv | 0.27 | 0.28 | 2 | |
rs8004738 | 0.925 | 0.080 | 14 | 94390577 | 5 prime UTR variant | G/A | snv | 0.55 | 2 | ||
rs3769839 | 0.925 | 0.080 | 2 | 230211910 | intron variant | T/C | snv | 0.12 | 2 | ||
rs1126580 | 0.882 | 0.120 | 2 | 218136243 | 3 prime UTR variant | G/A;T | snv | 3 | |||
rs3219476 | 0.882 | 0.200 | 1 | 45336998 | intron variant | A/C | snv | 0.58 | 3 | ||
rs3219472 | 0.882 | 0.160 | 1 | 45338378 | 5 prime UTR variant | C/T | snv | 0.26 | 3 | ||
rs11635252 | 0.925 | 0.080 | 15 | 90528542 | upstream gene variant | T/C | snv | 0.88 | 4 | ||
rs9679162 | 0.882 | 0.120 | 2 | 31024648 | intron variant | G/T | snv | 0.48 | 4 | ||
rs763569821 | 0.851 | 0.160 | 1 | 155188197 | missense variant | T/C | snv | 1.2E-05 | 4 | ||
rs2289278 | 0.827 | 0.200 | 5 | 111073450 | 5 prime UTR variant | C/G | snv | 8.7E-02 | 5 | ||
rs1126579 | 0.776 | 0.200 | 2 | 218136011 | 3 prime UTR variant | T/C | snv | 0.62 | 8 | ||
rs3024270 | 0.776 | 0.200 | 11 | 1996209 | non coding transcript exon variant | C/G;T | snv | 0.46; 5.2E-06 | 8 | ||
rs2106261 | 0.763 | 0.160 | 16 | 73017721 | intron variant | C/G;T | snv | 11 | |||
rs889312 | 0.732 | 0.360 | 5 | 56736057 | regulatory region variant | C/A | snv | 0.69 | 14 | ||
rs2287622 | 0.724 | 0.240 | 2 | 168973818 | missense variant | A/C;G;T | snv | 0.57 | 16 | ||
rs2072671 | 0.752 | 0.280 | 1 | 20589208 | missense variant | A/C | snv | 0.28 | 0.25 | 16 | |
rs3197999 | 0.732 | 0.280 | 3 | 49684099 | missense variant | G/A | snv | 0.26 | 0.27 | 16 | |
rs2266788 | 0.763 | 0.440 | 11 | 116789970 | 3 prime UTR variant | G/A | snv | 0.93 | 19 | ||
rs3740066 | 0.724 | 0.440 | 10 | 99844450 | missense variant | C/G;T | snv | 2.4E-05; 0.34 | 20 | ||
rs17851045 | 0.672 | 0.400 | 12 | 25227341 | missense variant | T/A;G | snv | 4.0E-06 | 27 |