Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3024994 | 0.776 | 0.120 | 6 | 43775770 | non coding transcript exon variant | C/T | snv | 3.8E-02 | 8 | ||
rs2498801 | 0.790 | 0.120 | 14 | 104769221 | upstream gene variant | T/C | snv | 0.41 | 7 | ||
rs937475913 | 0.790 | 0.120 | 8 | 47936435 | missense variant | T/C | snv | 4.0E-06 | 7 | ||
rs11191439 | 0.851 | 0.120 | 10 | 102878966 | missense variant | T/A;C | snv | 9.2E-02 | 6 | ||
rs798766 | 0.851 | 0.120 | 4 | 1732512 | intron variant | T/C | snv | 0.76 | 6 | ||
rs11892031 | 0.882 | 0.120 | 2 | 233656637 | intron variant | A/C;T | snv | 5 | |||
rs2292016 | 0.851 | 0.120 | 5 | 38845758 | non coding transcript exon variant | G/T | snv | 1.9E-02 | 5 | ||
rs3218373 | 0.827 | 0.120 | 7 | 152677078 | upstream gene variant | C/A | snv | 0.15 | 5 | ||
rs587783064 | 0.851 | 0.120 | 17 | 7669626 | missense variant | C/A;T | snv | 5 | |||
rs779682021 | 0.882 | 0.120 | 15 | 74721227 | missense variant | A/C | snv | 5 | |||
rs887569 | 0.882 | 0.120 | 7 | 148808210 | intron variant | C/T | snv | 0.73 | 5 | ||
rs10743980 | 0.882 | 0.120 | 12 | 12259861 | intron variant | T/A;C;G | snv | 4 | |||
rs2073859 | 0.882 | 0.120 | 22 | 31278567 | 3 prime UTR variant | G/A | snv | 4.0E-02 | 4 | ||
rs2278329 | 0.851 | 0.120 | 5 | 38921686 | missense variant | G/A | snv | 3.3E-02 | 2.2E-02 | 4 | |
rs1014971 | 0.882 | 0.120 | 22 | 38936618 | regulatory region variant | C/T | snv | 0.55 | 3 | ||
rs10234749 | 0.882 | 0.120 | 7 | 152690784 | regulatory region variant | T/C;G | snv | 3 | |||
rs10775480 | 0.882 | 0.120 | 18 | 45737317 | intron variant | T/C | snv | 0.61 | 3 | ||
rs11077654 | 0.882 | 0.120 | 17 | 73010373 | intron variant | A/C | snv | 0.69 | 3 | ||
rs11191438 | 0.882 | 0.120 | 10 | 102878107 | intron variant | G/A;C | snv | 3 | |||
rs1135612 | 0.882 | 0.120 | 7 | 75980359 | synonymous variant | A/G;T | snv | 0.28 | 3 | ||
rs11543198 | 0.882 | 0.120 | 15 | 74619987 | missense variant | G/A;T | snv | 0.11 | 3 | ||
rs11871756 | 0.882 | 0.120 | 17 | 72730105 | intron variant | C/G | snv | 0.11 | 3 | ||
rs1189516787 | 0.882 | 0.120 | 19 | 33301681 | missense variant | C/G | snv | 7.1E-06 | 3 | ||
rs1203030830 | 0.882 | 0.120 | 7 | 55155873 | synonymous variant | T/C | snv | 4.0E-06 | 3 | ||
rs1336331763 | 0.882 | 0.120 | 16 | 28606796 | missense variant | G/A | snv | 4.0E-06 | 3 |