Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9833888 | 1.000 | 0.080 | 3 | 100004736 | intron variant | G/T | snv | 0.18 | 1 | ||
rs1190983 | 0.925 | 0.080 | 14 | 100031649 | intron variant | T/C | snv | 0.61 | 2 | ||
rs9837602 | 1.000 | 0.080 | 3 | 100105841 | intron variant | G/A | snv | 0.18 | 1 | ||
rs181337095 | 1.000 | 0.080 | 15 | 100366889 | intergenic variant | G/A | snv | 1 | |||
rs2273802 | 0.925 | 0.080 | 14 | 100376562 | 5 prime UTR variant | G/A | snv | 0.33 | 2 | ||
rs612683 | 1.000 | 0.080 | 1 | 100414772 | intron variant | A/T | snv | 0.38 | 1 | ||
rs11292 | 0.925 | 0.080 | 10 | 100553850 | 3 prime UTR variant | A/G | snv | 0.22 | 2 | ||
rs17094222 | 0.925 | 0.080 | 10 | 100635683 | intergenic variant | T/C | snv | 0.17 | 3 | ||
rs10165970 | 0.708 | 0.320 | 2 | 100840527 | intron variant | G/A | snv | 0.16 | 18 | ||
rs17024869 | 0.708 | 0.320 | 2 | 100843581 | intron variant | T/C | snv | 8.3E-02 | 18 | ||
rs747097215 | 1.000 | 0.080 | 7 | 100856990 | missense variant | C/T | snv | 2.0E-05 | 2.1E-05 | 1 | |
rs17024926 | 0.851 | 0.120 | 2 | 100889540 | intron variant | T/C | snv | 0.34 | 4 | ||
rs895520 | 0.689 | 0.320 | 2 | 100961475 | intron variant | G/A | snv | 0.35 | 23 | ||
rs7581886 | 0.708 | 0.320 | 2 | 100964784 | intron variant | C/T | snv | 0.92 | 18 | ||
rs2305160 | 0.776 | 0.200 | 2 | 100974842 | missense variant | A/G | snv | 0.71 | 0.75 | 9 | |
rs4919510 | 0.641 | 0.520 | 10 | 100975021 | mature miRNA variant | C/G | snv | 0.27 | 0.27 | 32 | |
rs11541353 | 0.851 | 0.120 | 2 | 100977729 | missense variant | C/T | snv | 0.14 | 0.14 | 4 | |
rs3739008 | 0.925 | 0.080 | 2 | 100996106 | 3 prime UTR variant | C/T | snv | 0.24 | 2 | ||
rs500760 | 0.882 | 0.120 | 11 | 101039260 | synonymous variant | T/C | snv | 0.24 | 0.29 | 3 | |
rs10895054 | 0.925 | 0.080 | 11 | 101039579 | intron variant | A/T | snv | 0.11 | 2 | ||
rs575018 | 1.000 | 0.080 | 5 | 101043689 | intergenic variant | C/G;T | snv | 1 | |||
rs1042839 | 0.925 | 0.080 | 11 | 101051471 | synonymous variant | G/A | snv | 0.13 | 0.11 | 2 | |
rs56103835 | 0.925 | 0.080 | 14 | 101056219 | non coding transcript exon variant | T/A;C | snv | 4.0E-06; 0.28 | 2 | ||
rs1042838 | 0.742 | 0.240 | 11 | 101062681 | missense variant | C/A;G | snv | 0.13; 4.0E-06 | 12 | ||
rs590688 | 0.925 | 0.080 | 11 | 101105243 | intron variant | C/G | snv | 0.47 | 2 |