Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs778899140 | 0.925 | 6 | 165450268 | missense variant | T/C | snv | 4.0E-06 | 5 | |||
rs1057518011 | 1 | 1535766 | missense variant | C/T | snv | 4 | |||||
rs2161961 | 18 | 11774501 | intron variant | A/G | snv | 0.31 | 3 | ||||
rs875989839 | 1.000 | 6 | 165450242 | missense variant | C/G | snv | 3 | ||||
rs104895358 | 12 | 109595148 | missense variant | G/A | snv | 1.2E-05 | 2 | ||||
rs121912703 | 17 | 63496977 | missense variant | C/T | snv | 3.7E-05 | 4.9E-05 | 2 | |||
rs12765063 | 10 | 35127641 | intron variant | G/A | snv | 0.14 | 2 | ||||
rs402691 | 19 | 53888383 | intron variant | T/C | snv | 0.39 | 2 | ||||
rs1060504185 | 9 | 21971116 | missense variant | G/A;C | snv | 1 | |||||
rs1156401234 | 12 | 32740421 | missense variant | G/A | snv | 4.0E-06 | 1 | ||||
rs1334791875 | 21 | 25982369 | missense variant | G/A | snv | 4.0E-06 | 1 | ||||
rs1365502141 | 21 | 26000017 | missense variant | G/A | snv | 7.0E-06 | 1 | ||||
rs150450891 | 16 | 53826341 | missense variant | G/A | snv | 4.6E-04 | 5.7E-04 | 1 | |||
rs202064075 | 1 | 16048352 | missense variant | G/A | snv | 1.5E-04 | 7.7E-05 | 1 | |||
rs539815495 | 6 | 161973365 | missense variant | A/G | snv | 1.1E-04 | 1.4E-05 | 1 | |||
rs566794487 | 12 | 106997986 | missense variant | A/C | snv | 3.6E-05 | 1 | ||||
rs773857 | 19 | 16908042 | intron variant | C/T | snv | 0.56 | 1 | ||||
rs914655 | 9 | 16208133 | intron variant | G/T | snv | 1.6E-02 | 1 | ||||
rs2284411 | 1.000 | 0.040 | 12 | 13713238 | intron variant | C/T | snv | 0.34 | 4 | ||
rs6191 | 0.925 | 0.040 | 5 | 143278591 | 3 prime UTR variant | C/A | snv | 0.48 | 4 | ||
rs2110267 | 1.000 | 0.040 | 7 | 153838604 | intergenic variant | C/G | snv | 0.32 | 3 | ||
rs750257282 | 1.000 | 0.040 | 11 | 3038127 | missense variant | C/G;T | snv | 3.2E-05 | 3 | ||
rs945270 | 0.925 | 0.040 | 14 | 55733755 | intergenic variant | C/G;T | snv | 3 | |||
rs1170695 | 1.000 | 0.040 | 3 | 11013652 | 5 prime UTR variant | A/G | snv | 0.35 | 2 | ||
rs1541665 | 1.000 | 0.040 | 5 | 170715913 | intron variant | C/G;T | snv | 0.21 | 2 |