Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1052667 | 0.882 | 0.040 | 19 | 47004177 | 3 prime UTR variant | C/G;T | snv | 6 | |||
rs1005464 | 0.882 | 0.040 | 20 | 6775501 | intron variant | G/A | snv | 0.19 | 5 | ||
rs1226994105 | 0.882 | 0.040 | 7 | 106868379 | missense variant | G/A | snv | 8.0E-06 | 5 | ||
rs4150441 | 0.882 | 0.040 | 2 | 127283339 | intron variant | T/C | snv | 0.37 | 5 | ||
rs121913282 | 0.882 | 0.040 | 3 | 179221072 | missense variant | A/C | snv | 4 | |||
rs1690916 | 0.882 | 0.040 | 12 | 68841626 | 3 prime UTR variant | G/A | snv | 0.35 | 4 | ||
rs16948627 | 0.882 | 0.040 | 17 | 50063432 | intron variant | C/A;T | snv | 4 | |||
rs1906953 | 0.882 | 0.040 | 6 | 34068669 | intron variant | C/T | snv | 0.25 | 4 | ||
rs2230392 | 0.882 | 0.040 | 17 | 50078061 | missense variant | G/A | snv | 0.14 | 9.0E-02 | 4 | |
rs2285524 | 0.882 | 0.040 | 17 | 50073989 | synonymous variant | T/C | snv | 0.21 | 0.24 | 4 | |
rs7034162 | 0.882 | 0.040 | 9 | 14190288 | intron variant | A/T | snv | 0.81 | 4 | ||
rs7646409 | 0.882 | 0.040 | 3 | 179182405 | intron variant | T/C | snv | 0.26 | 4 | ||
rs876660254 | 0.882 | 0.040 | 17 | 7674963 | missense variant | G/T | snv | 4 | |||
rs10208273 | 0.882 | 0.040 | 2 | 6383862 | intergenic variant | A/G | snv | 0.30 | 3 | ||
rs1061970 | 0.882 | 0.040 | 17 | 50184491 | 3 prime UTR variant | A/G | snv | 0.13 | 3 | ||
rs11177386 | 0.882 | 0.040 | 12 | 68820362 | missense variant | G/A | snv | 3 | |||
rs1223868338 | 0.882 | 0.040 | 10 | 88990884 | missense variant | G/C | snv | 7.0E-06 | 3 | ||
rs12879262 | 0.882 | 0.040 | 14 | 102539710 | non coding transcript exon variant | G/C | snv | 0.12 | 0.11 | 3 | |
rs1295925 | 0.882 | 0.040 | 17 | 59832902 | intron variant | T/C | snv | 0.60 | 3 | ||
rs17111750 | 0.882 | 0.040 | 14 | 20442249 | downstream gene variant | C/T | snv | 0.30 | 3 | ||
rs17206779 | 0.882 | 0.040 | 5 | 65151950 | splice region variant | C/G;T | snv | 0.48 | 3 | ||
rs199812774 | 0.882 | 0.040 | 12 | 68839357 | synonymous variant | T/C | snv | 1.8E-04 | 2.4E-04 | 3 | |
rs201821879 | 0.882 | 0.040 | 12 | 68809237 | missense variant | C/T | snv | 1.6E-04 | 1.9E-04 | 3 | |
rs2075559 | 0.882 | 0.040 | 17 | 50189930 | intron variant | G/A;C;T | snv | 0.52; 4.0E-06 | 3 | ||
rs2236947 | 0.882 | 0.040 | 3 | 50334001 | intron variant | C/A | snv | 0.39 | 3 |