Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 1 | ||
rs2358994 | 0.925 | 0.120 | 1 | 113886839 | intron variant | G/A | snv | 0.16 | 2 | ||
rs7679475 | 0.925 | 0.120 | 4 | 121392885 | intergenic variant | A/C;G | snv | 2 | |||
rs2153977 | 0.807 | 0.240 | 1 | 113537449 | intron variant | C/T | snv | 0.28 | 2 | ||
rs2251396 | 0.827 | 0.240 | 6 | 31396930 | upstream gene variant | G/A | snv | 0.24 | 2 | ||
rs1015166 | 0.925 | 0.120 | 6 | 32830954 | intron variant | C/G;T | snv | 0.28 | 2 | ||
rs2523989 | 0.827 | 0.280 | 6 | 30110498 | missense variant | C/T | snv | 0.12 | 0.12 | 2 | |
rs11571297 | 0.882 | 0.120 | 2 | 203880280 | regulatory region variant | T/C | snv | 0.44 | 3 | ||
rs57348955 | 0.882 | 0.120 | 16 | 31174561 | upstream gene variant | G/A;C | snv | 3 | |||
rs1270942 | 0.742 | 0.440 | 6 | 31951083 | non coding transcript exon variant | A/G | snv | 7.5E-02 | 3 | ||
rs2270450 | 0.827 | 0.200 | 6 | 46677138 | 3 prime UTR variant | C/T | snv | 0.29 | 3 | ||
rs13093110 | 0.882 | 0.120 | 3 | 188407332 | intron variant | C/T | snv | 0.42 | 3 | ||
rs7537605 | 0.882 | 0.120 | 1 | 107800465 | intron variant | G/A;T | snv | 3 | |||
rs1980493 | 0.776 | 0.400 | 6 | 32395438 | intron variant | T/C | snv | 0.13 | 4 | ||
rs706779 | 0.827 | 0.160 | 10 | 6056861 | intron variant | T/C | snv | 0.48 | 4 | ||
rs886424 | 0.776 | 0.320 | 6 | 30814225 | non coding transcript exon variant | C/T | snv | 7.1E-02 | 8.7E-02 | 4 | |
rs1534422 | 0.827 | 0.160 | 2 | 12500615 | intron variant | G/A | snv | 0.52 | 4 | ||
rs2857595 | 0.827 | 0.320 | 6 | 31600692 | intergenic variant | G/A | snv | 0.27 | 5 | ||
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 6 | ||
rs4409785 | 0.752 | 0.240 | 11 | 95578258 | intron variant | T/C | snv | 0.13 | 12 | ||
rs10822050 | 0.724 | 0.240 | 10 | 62679011 | downstream gene variant | T/C | snv | 0.33 | 14 | ||
rs11839053 | 0.724 | 0.240 | 13 | 106410694 | intergenic variant | T/C | snv | 7.0E-02 | 14 | ||
rs12863738 | 0.724 | 0.240 | X | 136949968 | intron variant | C/T | snv | 0.16 | 14 | ||
rs1332099 | 0.724 | 0.240 | 10 | 99538694 | downstream gene variant | T/C;G | snv | 14 | |||
rs2075184 | 0.724 | 0.240 | 2 | 102464132 | intergenic variant | T/C | snv | 0.78 | 14 |