Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 24 | ||
rs34811474 | 1.000 | 0.040 | 4 | 25407216 | missense variant | G/A;T | snv | 0.15; 4.1E-06 | 8 | ||
rs10189857 | 1.000 | 0.080 | 2 | 60486100 | intron variant | A/G | snv | 0.42 | 5 | ||
rs1167827 | 7 | 75533848 | 3 prime UTR variant | G/A | snv | 0.37 | 5 | ||||
rs16978075 | 18 | 44533186 | intron variant | T/C | snv | 8.5E-02 | 5 | ||||
rs13212562 | 0.925 | 0.120 | 6 | 27332531 | intergenic variant | A/G | snv | 0.13 | 4 | ||
rs1569723 | 0.851 | 0.280 | 20 | 46113425 | upstream gene variant | C/A | snv | 0.80 | 4 | ||
rs2239647 | 0.851 | 0.080 | 14 | 32823537 | synonymous variant | A/C | snv | 0.60 | 0.65 | 4 | |
rs9388490 | 1.000 | 0.080 | 6 | 126383649 | intron variant | C/T | snv | 0.42 | 4 | ||
rs11171739 | 0.807 | 0.320 | 12 | 56076841 | 5 prime UTR variant | C/T | snv | 0.49 | 4 | ||
rs6704768 | 1.000 | 0.040 | 2 | 232727791 | intron variant | G/A | snv | 0.54 | 4 | ||
rs3751667 | 1.000 | 0.040 | 16 | 954554 | synonymous variant | C/T | snv | 0.28 | 0.29 | 4 | |
rs7832708 | 8 | 10332530 | intron variant | C/T | snv | 0.49 | 4 | ||||
rs71636784 | 1.000 | 0.040 | 1 | 26842709 | intron variant | T/G | snv | 0.12 | 4 | ||
rs78381888 | 0.925 | 0.040 | 2 | 96835038 | 3 prime UTR variant | A/G | snv | 0.13 | 3 | ||
rs72829446 | 17 | 7648805 | intron variant | C/T | snv | 6.5E-02 | 3 | ||||
rs2093210 | 1.000 | 0.040 | 14 | 60490561 | intron variant | C/T | snv | 0.45 | 3 | ||
rs10752262 | 1.000 | 0.040 | 10 | 12353101 | intron variant | C/T | snv | 0.39 | 3 | ||
rs12602286 | 1.000 | 0.040 | 17 | 19333641 | intron variant | G/T | snv | 0.79 | 3 | ||
rs2629540 | 0.925 | 0.080 | 10 | 124737579 | intron variant | G/C | snv | 0.18 | 3 | ||
rs9556958 | 1.000 | 0.040 | 13 | 98447792 | 3 prime UTR variant | C/G;T | snv | 3 | |||
rs2764261 | 6 | 108606639 | intron variant | A/G;T | snv | 3 | |||||
rs3747631 | 1.000 | 0.040 | 1 | 204618441 | missense variant | G/A;C | snv | 4.0E-06; 0.20 | 3 | ||
rs8067165 | 17 | 8128618 | upstream gene variant | C/A;G;T | snv | 3 | |||||
rs6731373 | 2 | 68275912 | intergenic variant | G/A | snv | 0.29 | 3 |