Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs41467651 | 0.925 | 0.080 | MT | 10310 | synonymous variant | G/A | snv | 2 | |||
rs8126 | 0.807 | 0.080 | 14 | 103137232 | 3 prime UTR variant | C/T | snv | 0.63 | 8 | ||
rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 104 | |
rs861528 | 0.925 | 0.080 | 14 | 103716661 | intron variant | C/T | snv | 0.17 | 2 | ||
rs2853826 | 0.925 | 0.080 | MT | 10398 | missense variant | A/G | snv | 2 | |||
rs28358278 | 0.925 | 0.080 | MT | 10400 | synonymous variant | C/T | snv | 2 | |||
rs12615966 | 0.882 | 0.080 | 2 | 104762499 | upstream gene variant | C/T | snv | 0.14 | 3 | ||
rs1130233 | 0.742 | 0.480 | 14 | 104773557 | synonymous variant | C/T | snv | 0.30 | 0.23 | 13 | |
rs2494752 | 0.790 | 0.120 | 14 | 104797271 | upstream gene variant | A/G | snv | 0.85 | 10 | ||
rs111638916 | 0.925 | 0.080 | X | 108084839 | 3 prime UTR variant | G/A | snv | 3 | |||
rs4444903 | 0.630 | 0.360 | 4 | 109912954 | 5 prime UTR variant | A/G | snv | 0.51 | 35 | ||
rs1279599 | 0.925 | 0.080 | 6 | 110879025 | intron variant | G/A | snv | 0.87 | 2 | ||
rs7768897 | 0.925 | 0.080 | 6 | 110891080 | non coding transcript exon variant | A/G;T | snv | 2 | |||
rs4938723 | 0.574 | 0.680 | 11 | 111511840 | intron variant | T/C | snv | 0.32 | 60 | ||
rs201745983 | 0.752 | 0.200 | 12 | 111783219 | missense variant | G/A | snv | 6.8E-05 | 7.7E-05 | 14 | |
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
rs16941667 | 0.925 | 0.080 | 12 | 111806609 | intron variant | C/T | snv | 8.6E-02 | 2 | ||
rs2074356 | 0.763 | 0.280 | 12 | 112207597 | intron variant | G/A | snv | 3.8E-03 | 18 | ||
rs1064261 | 0.925 | 0.080 | 1 | 11228701 | missense variant | G/A;T | snv | 0.75; 4.0E-06 | 3 | ||
rs11066280 | 0.742 | 0.280 | 12 | 112379979 | intron variant | T/A | snv | 7.0E-03 | 27 | ||
rs2301756 | 0.851 | 0.120 | 12 | 112452972 | intron variant | A/G | snv | 0.21 | 4 | ||
rs6968084 | 0.925 | 0.080 | 7 | 112457066 | missense variant | C/T | snv | 0.17 | 0.16 | 2 | |
rs3807213 | 0.882 | 0.200 | 7 | 112465699 | intron variant | G/T | snv | 0.57 | 3 | ||
rs12229892 | 0.807 | 0.240 | 12 | 112485589 | intron variant | G/A | snv | 1.4E-02 | 6 | ||
rs2295080 | 0.695 | 0.320 | 1 | 11262571 | upstream gene variant | G/C;T | snv | 20 |