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 | ||
rs1128249 | 1.000 | 0.080 | 2 | 164672114 | intron variant | G/C;T | snv | 9 | |||
rs2925979 | 1.000 | 0.080 | 16 | 81501185 | intron variant | T/A;C | snv | 9 | |||
rs7138803 | 0.827 | 0.240 | 12 | 49853685 | intergenic variant | G/A;T | snv | 9 | |||
rs12454712 | 0.925 | 0.120 | 18 | 63178651 | intron variant | T/A;C | snv | 7 | |||
rs2145272 | 20 | 6645571 | intergenic variant | G/A;T | snv | 7 | |||||
rs2283847 | 22 | 27785411 | intron variant | C/A;G;T | snv | 7 | |||||
rs1800978 | 1.000 | 0.040 | 9 | 104903697 | 5 prime UTR variant | C/A;G;T | snv | 5.4E-06; 0.14 | 6 | ||
rs6795735 | 0.882 | 0.120 | 3 | 64719689 | intron variant | C/A;G;T | snv | 6 | |||
rs1121980 | 0.807 | 0.240 | 16 | 53775335 | intron variant | G/A;C | snv | 5 | |||
rs12140153 | 1 | 62114219 | missense variant | G/A;T | snv | 4.0E-06; 5.9E-02 | 5 | ||||
rs13130484 | 1.000 | 0.080 | 4 | 45173674 | intergenic variant | C/A;T | snv | 5 | |||
rs2067087 | 1.000 | 0.080 | 7 | 27202041 | non coding transcript exon variant | G/C;T | snv | 5 | |||
rs7498665 | 0.925 | 0.120 | 16 | 28871920 | missense variant | A/G;T | snv | 0.35 | 5 | ||
rs10842707 | 12 | 26318431 | intron variant | C/G;T | snv | 4 | |||||
rs1443512 | 12 | 53948900 | downstream gene variant | A/C;T | snv | 4 | |||||
rs17819328 | 3 | 12447843 | intergenic variant | T/A;G | snv | 4 | |||||
rs1789882 | 1.000 | 0.080 | 4 | 99313896 | synonymous variant | A/G;T | snv | 0.82 | 4 | ||
rs2033529 | 6 | 40380914 | intron variant | A/C;G | snv | 4 | |||||
rs6545714 | 2 | 59080590 | intron variant | G/A;C | snv | 4 | |||||
rs8054556 | 0.925 | 0.080 | 16 | 29946895 | intron variant | G/A;C;T | snv | 4 | |||
rs887912 | 1.000 | 0.080 | 2 | 59075742 | intron variant | T/C;G | snv | 4 | |||
rs9435732 | 1 | 16981663 | intron variant | C/G;T | snv | 4 | |||||
rs9844972 | 1.000 | 0.080 | 3 | 150379848 | regulatory region variant | G/A;C | snv | 4 | |||
rs10980797 | 9 | 111150273 | intron variant | A/G;T | snv | 3 |