Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1004467 | 0.790 | 0.280 | 10 | 102834750 | non coding transcript exon variant | A/G | snv | 0.15 | 0.14 | 5 | |
rs10051330 | 5 | 158392616 | intron variant | A/G;T | snv | 2 | |||||
rs10059884 | 5 | 32832368 | regulatory region variant | C/A;T | snv | 5 | |||||
rs10060615 | 5 | 132373185 | intron variant | T/A;C | snv | 1 | |||||
rs10062049 | 5 | 62258054 | regulatory region variant | C/T | snv | 0.16 | 2 | ||||
rs10077885 | 5 | 115054424 | regulatory region variant | C/A | snv | 0.56 | 2 | ||||
rs10078021 | 5 | 75742606 | intergenic variant | T/G | snv | 0.51 | 1 | ||||
rs10087782 | 8 | 140848521 | intron variant | T/C | snv | 0.43 | 1 | ||||
rs10092965 | 8 | 8515975 | intergenic variant | A/G | snv | 0.43 | 2 | ||||
rs10103353 | 8 | 81937217 | intergenic variant | C/T | snv | 0.35 | 1 | ||||
rs1015291 | 12 | 19831845 | intron variant | A/G | snv | 0.55 | 1 | ||||
rs1015538 | 7 | 100028412 | intron variant | A/G | snv | 0.72 | 1 | ||||
rs10164193 | 18 | 33581462 | intron variant | T/G | snv | 0.13 | 1 | ||||
rs10166552 | 2 | 223171819 | intron variant | C/A;G;T | snv | 4.3E-03 | 2 | ||||
rs10176996 | 2 | 19508931 | intron variant | C/T | snv | 0.69 | 1 | ||||
rs10184428 | 2 | 164155317 | intron variant | C/A;G | snv | 5 | |||||
rs10184839 | 2 | 181081388 | intron variant | A/T | snv | 0.77 | 1 | ||||
rs10193543 | 2 | 72256200 | intron variant | T/G | snv | 0.13 | 1 | ||||
rs10198275 | 2 | 24907673 | intron variant | A/C | snv | 0.53 | 1 | ||||
rs10224002 | 0.925 | 0.080 | 7 | 151717955 | intron variant | A/G | snv | 0.31 | 8 | ||
rs10228276 | 7 | 27207660 | downstream gene variant | G/A | snv | 0.73 | 1 | ||||
rs10255839 | 7 | 27249498 | intron variant | G/A | snv | 0.87 | 6 | ||||
rs10260816 | 7 | 45970501 | intron variant | C/A;G;T | snv | 2 | |||||
rs10275663 | 7 | 50729988 | intron variant | G/A | snv | 9.4E-02 | 2 | ||||
rs1027989 | 8 | 55901862 | intron variant | G/A;C | snv | 3 |