Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10054063 | 5 | 173965395 | downstream gene variant | A/T | snv | 0.26 | 4 | ||||
rs10185855 | 2 | 101025798 | intron variant | A/G | snv | 0.35 | 4 | ||||
rs10401969 | 0.776 | 0.240 | 19 | 19296909 | intron variant | T/C | snv | 0.10 | 22 | ||
rs10408163 | 19 | 47093845 | non coding transcript exon variant | T/C | snv | 0.52 | 6 | ||||
rs1041968 | 2 | 21009932 | synonymous variant | G/A | snv | 0.39 | 0.38 | 4 | |||
rs1042034 | 0.851 | 0.240 | 2 | 21002409 | missense variant | C/T | snv | 0.70 | 0.78 | 6 | |
rs10468017 | 0.851 | 0.120 | 15 | 58386313 | intron variant | C/T | snv | 0.24 | 6 | ||
rs1077834 | 15 | 58431280 | intron variant | T/C | snv | 0.34 | 4 | ||||
rs1077835 | 15 | 58431227 | intron variant | A/G | snv | 0.34 | 3 | ||||
rs10808546 | 8 | 125483576 | intron variant | C/T | snv | 0.39 | 6 | ||||
rs10832027 | 11 | 13335636 | intron variant | G/A | snv | 0.67 | 5 | ||||
rs10876041 | 12 | 50508099 | intron variant | T/C | snv | 0.58 | 4 | ||||
rs10889348 | 1 | 62612551 | intron variant | A/T | snv | 0.32 | 3 | ||||
rs10889353 | 1 | 62652525 | intron variant | A/C;T | snv | 4 | |||||
rs10900522 | 1 | 205714939 | 3 prime UTR variant | T/C | snv | 0.21 | 4 | ||||
rs11048456 | 1.000 | 0.080 | 12 | 26310149 | intron variant | C/T | snv | 0.62 | 6 | ||
rs11079810 | 17 | 48150484 | intron variant | C/T | snv | 0.16 | 4 | ||||
rs11207995 | 1 | 62583880 | intron variant | A/C;G | snv | 3 | |||||
rs112875651 | 8 | 125494452 | intron variant | G/A | snv | 0.31 | 7 | ||||
rs1129555 | 10 | 112150963 | 3 prime UTR variant | A/G | snv | 0.71 | 5 | ||||
rs11340914 | 1 | 23421504 | intron variant | AA/-;A;AAA | delins | 0.65 | 2 | ||||
rs115485095 | 6 | 31888293 | intron variant | G/A | snv | 3 | |||||
rs115845232 | 6 | 31304484 | intron variant | C/T | snv | 3 | |||||
rs11604424 | 11 | 116780399 | intron variant | C/G;T | snv | 3 | |||||
rs116477171 | 6 | 31918153 | intron variant | C/G;T | snv | 3 |