Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1052553 | 0.827 | 0.200 | 17 | 45996523 | synonymous variant | A/G | snv | 0.14 | 0.15 | 8 | |
rs1053924 | 1.000 | 0.120 | 6 | 32152938 | non coding transcript exon variant | T/C | snv | 0.71 | 1 | ||
rs1055271 | 1.000 | 0.120 | 22 | 50489911 | 3 prime UTR variant | G/C | snv | 0.27 | 1 | ||
rs1055569 | 0.882 | 0.240 | 6 | 31472305 | non coding transcript exon variant | C/T | snv | 0.41 | 3 | ||
rs1058026 | 0.925 | 0.120 | 6 | 31353908 | 3 prime UTR variant | A/C | snv | 0.21 | 5 | ||
rs1063856 | 0.763 | 0.400 | 12 | 6044368 | missense variant | T/C;G | snv | 0.31 | 14 | ||
rs1065356 | 1.000 | 0.120 | 6 | 31719231 | synonymous variant | G/A | snv | 0.27 | 0.31 | 1 | |
rs10735810 | 0.662 | 0.640 | 12 | 47879112 | start lost | A/C;G;T | snv | 26 | |||
rs10741657 | 0.637 | 0.520 | 11 | 14893332 | upstream gene variant | A/G | snv | 0.65 | 34 | ||
rs10743152 | 1.000 | 0.120 | 11 | 2174751 | upstream gene variant | T/C | snv | 0.63 | 1 | ||
rs10758593 | 0.827 | 0.240 | 9 | 4292083 | intron variant | G/A | snv | 0.45 | 8 | ||
rs10766196 | 0.925 | 0.120 | 11 | 14891585 | 5 prime UTR variant | A/G | snv | 0.35 | 2 | ||
rs10770125 | 0.882 | 0.200 | 11 | 2147784 | missense variant | A/G | snv | 0.49 | 0.40 | 4 | |
rs10770141 | 1.000 | 0.120 | 11 | 2172610 | upstream gene variant | A/C;G | snv | 2 | |||
rs1077393 | 0.882 | 0.200 | 6 | 31642752 | non coding transcript exon variant | A/G | snv | 0.44 | 3 | ||
rs10774654 | 1.000 | 0.120 | 12 | 112525756 | intergenic variant | A/G | snv | 0.20 | 1 | ||
rs10774671 | 0.732 | 0.480 | 12 | 112919388 | splice acceptor variant | G/A;C | snv | 0.67 | 14 | ||
rs10786436 | 1.000 | 0.120 | 10 | 98540425 | intron variant | C/T | snv | 0.40 | 1 | ||
rs10795791 | 0.925 | 0.200 | 10 | 6066377 | upstream gene variant | A/G | snv | 0.40 | 2 | ||
rs10807113 | 1.000 | 0.120 | 6 | 32754409 | upstream gene variant | C/A;G | snv | 1 | |||
rs10810632 | 1.000 | 0.120 | 9 | 16789026 | intron variant | C/T | snv | 0.85 | 1 | ||
rs10811661 | 0.724 | 0.400 | 9 | 22134095 | intergenic variant | T/C | snv | 0.14 | 22 | ||
rs10822050 | 0.724 | 0.240 | 10 | 62679011 | downstream gene variant | T/C | snv | 0.33 | 14 | ||
rs10850053 | 1.000 | 0.120 | 12 | 112539973 | regulatory region variant | T/C | snv | 0.19 | 1 | ||
rs10889677 | 0.627 | 0.720 | 1 | 67259437 | 3 prime UTR variant | C/A | snv | 0.27 | 40 |