Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs629301 | 0.851 | 0.120 | 1 | 109275684 | 3 prime UTR variant | G/T | snv | 0.74 | 19 | ||
rs646776 | 0.752 | 0.240 | 1 | 109275908 | downstream gene variant | C/T | snv | 0.74 | 10 | ||
rs12740374 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 9 | ||
rs7528419 | 0.851 | 0.080 | 1 | 109274570 | 3 prime UTR variant | A/G | snv | 0.23 | 9 | ||
rs11591147 | 0.677 | 0.360 | 1 | 55039974 | missense variant | G/A;T | snv | 1.2E-02 | 6 | ||
rs12748152 | 1.000 | 0.120 | 1 | 26811902 | upstream gene variant | C/T | snv | 5.7E-02 | 6 | ||
rs2642438 | 1 | 220796686 | missense variant | A/G | snv | 0.75 | 0.78 | 6 | |||
rs599839 | 0.724 | 0.360 | 1 | 109279544 | downstream gene variant | G/A;C | snv | 6 | |||
rs114165349 | 1 | 26695422 | intron variant | G/C | snv | 1.7E-02 | 5 | ||||
rs79598313 | 1 | 26958422 | intron variant | C/A;T | snv | 5 | |||||
rs10889353 | 1 | 62652525 | intron variant | A/C;T | snv | 4 | |||||
rs10900522 | 1 | 205714939 | 3 prime UTR variant | T/C | snv | 0.21 | 4 | ||||
rs11206510 | 0.763 | 0.240 | 1 | 55030366 | intergenic variant | T/A;C;G | snv | 4 | |||
rs1167998 | 1 | 62465961 | intron variant | C/A | snv | 0.57 | 4 | ||||
rs1748195 | 0.851 | 0.120 | 1 | 62583922 | intron variant | C/G;T | snv | 4 | |||
rs3761959 | 0.827 | 0.320 | 1 | 157699488 | intron variant | C/A;G;T | snv | 4 | |||
rs4495740 | 1 | 62658794 | intron variant | T/G | snv | 0.34 | 4 | ||||
rs586178 | 1 | 25420739 | missense variant | G/A;C | snv | 8.4E-05; 0.41 | 4 | ||||
rs10889348 | 1 | 62612551 | intron variant | A/T | snv | 0.32 | 3 | ||||
rs10903129 | 1 | 25442446 | intron variant | A/G | snv | 0.58 | 3 | ||||
rs11207995 | 1 | 62583880 | intron variant | A/C;G | snv | 3 | |||||
rs1168013 | 1.000 | 0.120 | 1 | 62531167 | intron variant | C/G;T | snv | 3 | |||
rs12042319 | 1.000 | 0.040 | 1 | 62584148 | 3 prime UTR variant | G/A | snv | 0.36 | 3 | ||
rs12047226 | 1 | 62639867 | intron variant | T/A;C | snv | 3 | |||||
rs1689788 | 1 | 182175287 | intron variant | T/C | snv | 0.29 | 3 |