Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1003346 | 1.000 | 9 | 109053060 | intron variant | C/A | snv | 0.43 | 2 | |||
rs10033464 | 0.807 | 0.200 | 4 | 110799605 | downstream gene variant | T/G | snv | 0.86 | 8 | ||
rs10089084 | 8 | 39912430 | intron variant | G/C | snv | 0.30 | 1 | ||||
rs1010 | 0.807 | 0.120 | 2 | 85581859 | 3 prime UTR variant | T/C;G | snv | 7 | |||
rs10118757 | 0.827 | 0.120 | 9 | 21853340 | intron variant | A/G | snv | 0.26 | 7 | ||
rs10123021 | 9 | 100689786 | regulatory region variant | G/A;T | snv | 1 | |||||
rs1035543 | 16 | 71949873 | missense variant | G/C | snv | 0.39 | 0.33 | 2 | |||
rs10401969 | 0.776 | 0.240 | 19 | 19296909 | intron variant | T/C | snv | 0.10 | 25 | ||
rs10414398 | 19 | 44517149 | missense variant | G/A | snv | 0.14 | 0.15 | 1 | |||
rs1041740 | 0.807 | 0.320 | 21 | 31667849 | intron variant | C/T | snv | 0.24 | 8 | ||
rs10423928 | 0.807 | 0.200 | 19 | 45679046 | intron variant | T/A | snv | 0.19 | 12 | ||
rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
rs1042579 | 0.732 | 0.240 | 20 | 23048087 | missense variant | G/A;T | snv | 0.19 | 16 | ||
rs1042713 | 0.576 | 0.800 | 5 | 148826877 | missense variant | G/A | snv | 0.42 | 0.43 | 63 | |
rs1042714 | 0.597 | 0.640 | 5 | 148826910 | stop gained | G/C;T | snv | 0.68 | 54 | ||
rs10432782 | 0.807 | 0.160 | 21 | 31664078 | intron variant | T/G | snv | 0.19 | 7 | ||
rs10435816 | 1.000 | 0.080 | 9 | 6225535 | intron variant | A/G | snv | 0.35 | 2 | ||
rs1043994 | 0.827 | 0.120 | 19 | 15192033 | synonymous variant | T/A;C | snv | 4.0E-06; 0.85 | 7 | ||
rs1044498 | 0.752 | 0.360 | 6 | 131851228 | missense variant | A/C;G | snv | 0.19 | 15 | ||
rs10455872 | 0.662 | 0.320 | 6 | 160589086 | intron variant | A/G | snv | 4.3E-02 | 33 | ||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs10478723 | 6 | 12295228 | intron variant | G/A | snv | 0.15 | 1 | ||||
rs1048661 | 0.732 | 0.320 | 15 | 73927205 | missense variant | G/T | snv | 0.33 | 0.28 | 14 | |
rs10488682 | 1.000 | 0.160 | 11 | 18040935 | 5 prime UTR variant | T/A | snv | 0.19 | 2 | ||
rs104894845 | 0.807 | 0.160 | X | 101401752 | missense variant | C/G;T | snv | 5.5E-04 | 8 |