Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs132793 | 0.851 | 0.160 | 22 | 41667677 | downstream gene variant | A/C;G;T | snv | 7 | |||
rs7859384 | 0.882 | 0.120 | 9 | 79507370 | intron variant | A/C;G | snv | 6 | |||
rs11813268 | 0.925 | 0.120 | 10 | 103922538 | upstream gene variant | C/T | snv | 0.31 | 2 | ||
rs1417080 | 0.925 | 0.120 | 9 | 79515946 | non coding transcript exon variant | T/C | snv | 0.35 | 2 | ||
rs3118523 | 0.925 | 0.120 | 9 | 134443675 | downstream gene variant | G/A | snv | 0.75 | 2 | ||
rs6466135 | 0.925 | 0.120 | 7 | 106861053 | upstream gene variant | A/G | snv | 0.71 | 2 | ||
rs7132434 | 0.925 | 0.120 | 12 | 26319629 | non coding transcript exon variant | A/G | snv | 0.62 | 2 | ||
rs748964 | 0.925 | 0.120 | 9 | 134442243 | downstream gene variant | C/G;T | snv | 2 | |||
rs2231142 | 0.583 | 0.680 | 4 | 88131171 | missense variant | G/C;T | snv | 4.0E-06; 0.12 | 56 | ||
rs1154454 | 0.925 | 0.120 | 4 | 99417185 | intron variant | A/G | snv | 0.22 | 2 | ||
rs266729 | 0.637 | 0.560 | 3 | 186841685 | upstream gene variant | C/A;G;T | snv | 37 | |||
rs182052 | 0.701 | 0.440 | 3 | 186842993 | intron variant | G/A | snv | 0.38 | 19 | ||
rs3774262 | 0.851 | 0.200 | 3 | 186854025 | intron variant | G/A | snv | 0.10 | 5 | ||
rs1800435 | 0.827 | 0.200 | 9 | 113391611 | missense variant | C/G | snv | 8.3E-02 | 6.1E-02 | 7 | |
rs2761016 | 0.925 | 0.120 | 9 | 113391072 | intron variant | T/C | snv | 0.59 | 2 | ||
rs1048798213 | 1.000 | 0.120 | 5 | 112837872 | missense variant | C/G | snv | 1 | |||
rs1442780982 | 1.000 | 0.120 | 5 | 112837977 | missense variant | C/A;G;T | snv | 4.0E-06 | 1 | ||
rs1130409 | 0.555 | 0.720 | 14 | 20456995 | missense variant | T/A;C;G | snv | 4.0E-06; 4.0E-06; 0.42 | 72 | ||
rs405509 | 0.667 | 0.480 | 19 | 44905579 | upstream gene variant | T/G | snv | 0.58 | 30 | ||
rs12553173 | 1.000 | 0.120 | 9 | 35674104 | synonymous variant | T/C | snv | 0.14 | 0.20 | 1 | |
rs2606736 | 1.000 | 0.120 | 3 | 11358775 | intron variant | C/A;T | snv | 4 | |||
rs6442260 | 0.925 | 0.160 | 3 | 11549277 | intron variant | G/A | snv | 0.42 | 2 | ||
rs611646 | 0.882 | 0.120 | 11 | 108306370 | intron variant | T/A;C | snv | 3 | |||
rs750597831 | 1.000 | 0.120 | 11 | 108229230 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 2 | |
rs587782274 | 1.000 | 0.120 | 11 | 108312465 | missense variant | A/C | snv | 1 |