Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs78154696 | 1.000 | 0.080 | 5 | 1000041 | upstream gene variant | G/A;T | snv | 1 | |||
rs3131837 | 0.882 | 0.080 | 1 | 100252204 | non coding transcript exon variant | C/G | snv | 0.80 | 3 | ||
rs7534220 | 1.000 | 0.080 | 1 | 100258911 | non coding transcript exon variant | T/A;C | snv | 1 | |||
rs79398649 | 1.000 | 0.080 | 5 | 1004587 | upstream gene variant | G/T | snv | 6.7E-02 | 1 | ||
rs7158663 | 0.827 | 0.240 | 14 | 100853087 | non coding transcript exon variant | A/G | snv | 0.42 | 9 | ||
rs4081134 | 0.790 | 0.160 | 14 | 100855451 | non coding transcript exon variant | G/A | snv | 0.29 | 7 | ||
rs1174612410 | 0.882 | 0.080 | 7 | 100860016 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 3 | |
rs62621207 | 1.000 | 0.080 | 10 | 100912491 | non coding transcript exon variant | A/T | snv | 3.0E-02 | 1 | ||
rs4919510 | 0.641 | 0.520 | 10 | 100975021 | mature miRNA variant | C/G | snv | 0.27 | 0.27 | 32 | |
rs12894467 | 0.807 | 0.080 | 14 | 101041390 | non coding transcript exon variant | C/T | snv | 0.51 | 0.50 | 6 | |
rs1799889 | 0.649 | 0.600 | 7 | 101126430 | upstream gene variant | A/G | snv | 31 | |||
rs6092 | 0.807 | 0.200 | 7 | 101128436 | missense variant | G/A | snv | 9.5E-02 | 8.0E-02 | 6 | |
rs3218977 | 0.807 | 0.240 | 2 | 102024739 | 3 prime UTR variant | A/G | snv | 0.14 | 6 | ||
rs2072472 | 0.732 | 0.200 | 2 | 102026557 | intron variant | A/G | snv | 0.24 | 13 | ||
rs1416580204 | 0.608 | 0.720 | 14 | 102250837 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 49 | |
rs28362491 | 0.592 | 0.720 | 4 | 102500998 | non coding transcript exon variant | ATTG/- | delins | 56 | |||
rs3774934 | 0.851 | 0.080 | 4 | 102506319 | intron variant | A/C;G;T | snv | 4 | |||
rs13117745 | 0.882 | 0.080 | 4 | 102557546 | intron variant | C/T | snv | 0.18 | 3 | ||
rs230541 | 0.882 | 0.080 | 4 | 102576628 | intron variant | G/A | snv | 0.58 | 3 | ||
rs1801 | 0.882 | 0.080 | 4 | 102579897 | intron variant | C/G;T | snv | 3 | |||
rs4648127 | 0.882 | 0.080 | 4 | 102614748 | intron variant | C/T | snv | 4.3E-02 | 3 | ||
rs35866072 | 0.716 | 0.360 | 11 | 102713373 | missense variant | T/G | snv | 6.0E-02 | 9.8E-02 | 17 | |
rs34009635 | 0.716 | 0.360 | 11 | 102713445 | missense variant | A/G | snv | 2.5E-03 | 6.2E-04 | 17 | |
rs1144393 | 0.851 | 0.160 | 11 | 102798678 | intron variant | T/C | snv | 0.30 | 5 | ||
rs1799750 | 0.592 | 0.760 | 11 | 102799765 | intron variant | C/- | delins | 0.50 | 48 |