Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2647012 | 0.790 | 0.320 | 6 | 32696681 | intergenic variant | T/C | snv | 0.64 | 7 | ||
rs1456896 | 0.882 | 0.200 | 7 | 50264865 | upstream gene variant | C/T | snv | 0.67 | 5 | ||
rs1364989 | 0.925 | 0.160 | 4 | 54145602 | intron variant | T/C | snv | 0.73 | 2 | ||
rs601162 | 0.925 | 0.160 | 9 | 29632144 | upstream gene variant | A/C;G;T | snv | 2 | |||
rs6697139 | 0.925 | 0.160 | 1 | 161690906 | intergenic variant | G/A;T | snv | 2 | |||
rs7692514 | 0.925 | 0.160 | 4 | 65276878 | intergenic variant | G/A;C | snv | 2 | |||
rs7773456 | 0.925 | 0.160 | 6 | 19823007 | intron variant | T/G | snv | 0.35 | 2 | ||
rs17008504 | 1.000 | 0.160 | 4 | 124718662 | intergenic variant | T/A | snv | 4.3E-02 | 1 | ||
rs1267969615 | 0.532 | 0.760 | 17 | 63490960 | missense variant | T/C | snv | 4.0E-06 | 100 | ||
rs2271100 | 1.000 | 0.160 | 4 | 177438525 | intron variant | T/C | snv | 0.19 | 1 | ||
rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 134 | |
rs172378 | 0.790 | 0.240 | 1 | 22638945 | synonymous variant | A/G | snv | 0.49 | 0.51 | 11 | |
rs292001 | 0.807 | 0.320 | 1 | 22638465 | intron variant | G/A | snv | 0.54 | 6 | ||
rs1108131 | 0.925 | 0.160 | 10 | 12455748 | intron variant | T/C | snv | 0.28 | 2 | ||
rs2246614 | 0.882 | 0.160 | 11 | 619789 | missense variant | T/G | snv | 0.63 | 0.59 | 3 | |
rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 72 | |
rs800292 | 0.645 | 0.560 | 1 | 196673103 | missense variant | G/A | snv | 0.32 | 0.40 | 33 | |
rs6677604 | 0.827 | 0.200 | 1 | 196717788 | intron variant | G/A | snv | 0.23 | 7 | ||
rs2295415 | 0.882 | 0.160 | 10 | 35212510 | 3 prime UTR variant | A/G | snv | 0.19 | 3 | ||
rs2298804 | 0.851 | 0.240 | 1 | 159304102 | missense variant | A/G;T | snv | 6.6E-03 | 4 | ||
rs396991 | 0.742 | 0.480 | 1 | 161544752 | missense variant | A/C;G;T | snv | 0.33; 4.1E-06 | 14 | ||
rs10127939 | 0.851 | 0.160 | 1 | 161548543 | missense variant | A/C;T | snv | 4.3E-02; 5.5E-02 | 5 | ||
rs3824662 | 0.752 | 0.320 | 10 | 8062245 | intron variant | C/A;T | snv | 11 | |||
rs2275913 | 0.514 | 0.760 | 6 | 52186235 | upstream gene variant | G/A | snv | 0.28 | 105 | ||
rs8193037 | 0.752 | 0.320 | 6 | 52186311 | upstream gene variant | G/A;T | snv | 12 |