Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1001179 | 0.641 | 0.680 | 11 | 34438684 | upstream gene variant | C/T | snv | 0.16 | 33 | ||
rs10012 | 0.716 | 0.280 | 2 | 38075247 | missense variant | G/C | snv | 0.31 | 0.36 | 16 | |
rs10022462 | 1.000 | 0.080 | 4 | 88322666 | intron variant | C/T | snv | 0.41 | 1 | ||
rs1003623 | 0.925 | 0.080 | 11 | 108281855 | intron variant | C/G;T | snv | 2 | |||
rs10043985 | 0.925 | 0.080 | 5 | 111065770 | upstream gene variant | A/C | snv | 5.2E-02 | 2 | ||
rs10046 | 0.708 | 0.400 | 15 | 51210789 | 3 prime UTR variant | G/A | snv | 0.45 | 0.43 | 18 | |
rs1004982 | 0.925 | 0.080 | 15 | 51321614 | non coding transcript exon variant | T/C;G | snv | 2 | |||
rs10053538 | 0.807 | 0.160 | 5 | 157110499 | intron variant | C/A;T | snv | 7 | |||
rs10057194 | 0.925 | 0.080 | 5 | 83362752 | intergenic variant | A/G | snv | 0.16 | 2 | ||
rs10069690 | 0.595 | 0.560 | 5 | 1279675 | intron variant | C/T | snv | 0.36 | 53 | ||
rs10077427 | 0.925 | 0.080 | 5 | 75542076 | intron variant | A/G | snv | 0.13 | 2 | ||
rs1008805 | 0.851 | 0.160 | 15 | 51257402 | intron variant | G/A | snv | 0.64 | 7 | ||
rs10090154 | 0.807 | 0.160 | 8 | 127519892 | intergenic variant | T/A;C | snv | 7 | |||
rs10096351 | 1.000 | 0.080 | 8 | 127359926 | intron variant | A/G | snv | 0.60 | 1 | ||
rs10109984 | 0.925 | 0.080 | 8 | 47891114 | intron variant | T/C | snv | 0.54 | 4 | ||
rs1011329790 | 0.925 | 0.080 | 7 | 30504681 | missense variant | G/A | snv | 3 | |||
rs1011970 | 0.677 | 0.320 | 9 | 22062135 | intron variant | G/T | snv | 0.23 | 22 | ||
rs1012477 | 0.827 | 0.160 | 1 | 7798075 | intron variant | G/C | snv | 0.16 | 8 | ||
rs10145182 | 0.925 | 0.080 | 14 | 50809291 | intron variant | T/A;C;G | snv | 2 | |||
rs10146997 | 0.827 | 0.240 | 14 | 79478819 | intron variant | A/G | snv | 0.25 | 6 | ||
rs10165970 | 0.708 | 0.320 | 2 | 100840527 | intron variant | G/A | snv | 0.16 | 18 | ||
rs10169133 | 1.000 | 0.080 | 2 | 19212878 | intron variant | G/C;T | snv | 0.55 | 1 | ||
rs10169372 | 0.925 | 0.080 | 2 | 217006626 | intergenic variant | A/G;T | snv | 2 | |||
rs1017105 | 0.925 | 0.080 | 7 | 90413990 | 3 prime UTR variant | C/T | snv | 0.29 | 2 | ||
rs1017226 | 0.925 | 0.080 | 5 | 56857565 | intron variant | T/C | snv | 5.8E-02 | 2 |