Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6498486 | 0.776 | 0.200 | 16 | 13919809 | upstream gene variant | A/C | snv | 0.27 | 8 | ||
rs1917799 | 0.851 | 0.120 | 10 | 49542929 | upstream gene variant | A/C | snv | 0.25 | 4 | ||
rs7749023 | 1.000 | 0.040 | 6 | 42093995 | non coding transcript exon variant | A/C;T | snv | 1 | |||
rs1695 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 188 | |
rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 108 | ||
rs2301756 | 0.851 | 0.120 | 12 | 112452972 | intron variant | A/G | snv | 0.21 | 4 | ||
rs158916 | 0.882 | 0.080 | 5 | 60949318 | intron variant | A/G | snv | 0.15 | 3 | ||
rs3814896 | 0.882 | 0.080 | 21 | 42351602 | upstream gene variant | A/G | snv | 0.17 | 3 | ||
rs2014486 | 1.000 | 0.040 | 11 | 1237573 | intron variant | A/G | snv | 0.52 | 2 | ||
rs7747696 | 1.000 | 0.040 | 6 | 42093217 | non coding transcript exon variant | A/G | snv | 0.54 | 1 | ||
rs760805 | 0.776 | 0.240 | 1 | 24925432 | intron variant | A/T | snv | 0.42 | 9 | ||
rs6672420 | 0.827 | 0.120 | 1 | 24964519 | missense variant | A/T | snv | 0.56 | 0.50 | 6 | |
rs629367 | 0.776 | 0.200 | 11 | 122146306 | intron variant | C/A | snv | 0.88 | 11 | ||
rs11536878 | 0.827 | 0.240 | 9 | 117709275 | intron variant | C/A | snv | 9.5E-02 | 5 | ||
rs121434254 | 0.807 | 0.200 | 21 | 44289773 | stop gained | C/A;T | snv | 7.5E-04 | 6 | ||
rs2910164 | 0.447 | 0.880 | 5 | 160485411 | mature miRNA variant | C/G | snv | 0.71; 4.1E-06 | 0.70 | 193 | |
rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 | |
rs2607775 | 0.807 | 0.160 | 3 | 14178595 | 5 prime UTR variant | C/G | snv | 0.42 | 0.43 | 8 | |
rs4711690 | 0.882 | 0.080 | 6 | 41741200 | missense variant | C/G | snv | 0.19 | 0.20 | 3 | |
rs3789210 | 0.882 | 0.080 | 6 | 41743584 | intron variant | C/G;T | snv | 3 | |||
rs765803011 | 1.000 | 0.040 | 16 | 27363094 | missense variant | C/G;T | snv | 4.0E-06; 1.6E-05 | 1 | ||
rs4986791 | 0.456 | 0.840 | 9 | 117713324 | missense variant | C/T | snv | 5.7E-02 | 4.9E-02 | 182 | |
rs2294008 | 0.672 | 0.320 | 8 | 142680513 | 5 prime UTR variant | C/T | snv | 0.46 | 0.45 | 28 | |
rs2094258 | 0.701 | 0.280 | 13 | 102844409 | intron variant | C/T | snv | 0.18 | 20 | ||
rs1130233 | 0.742 | 0.480 | 14 | 104773557 | synonymous variant | C/T | snv | 0.30 | 0.23 | 13 |