Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4149056 | 0.633 | 0.480 | 12 | 21178615 | missense variant | T/C | snv | 0.13 | 0.12 | 45 | |
rs780093 | 0.763 | 0.240 | 2 | 27519736 | intron variant | T/C | snv | 0.68 | 30 | ||
rs1625895 | 0.752 | 0.200 | 17 | 7674797 | non coding transcript exon variant | T/A;C;G | snv | 9.1E-06; 0.86; 4.5E-06 | 13 | ||
rs727428 | 0.882 | 0.200 | 17 | 7634474 | downstream gene variant | T/C | snv | 0.55 | 11 | ||
rs727479 | 0.790 | 0.240 | 15 | 51242350 | intron variant | C/A;T | snv | 10 | |||
rs12150660 | 1.000 | 0.040 | 17 | 7618597 | intron variant | G/T | snv | 0.17 | 5 | ||
rs6258 | 1.000 | 0.040 | 17 | 7631360 | missense variant | C/A;T | snv | 5.6E-05; 4.5E-03 | 5 | ||
rs9901675 | 17 | 7581494 | missense variant | G/A | snv | 5.4E-02 | 5.5E-02 | 5 | |||
rs12591359 | 0.925 | 0.080 | 15 | 51247171 | intron variant | G/A | snv | 0.41 | 4 | ||
rs2414095 | 15 | 51232095 | intron variant | A/G | snv | 0.69 | 4 | ||||
rs2445762 | 1.000 | 0.080 | 15 | 51325511 | intron variant | T/C | snv | 0.31 | 4 | ||
rs10454142 | 2 | 48419260 | intergenic variant | T/C | snv | 0.22 | 3 | ||||
rs10514317 | 5 | 89813933 | intergenic variant | C/A;T | snv | 3 | |||||
rs117585797 | 12 | 5902324 | intron variant | C/A | snv | 1.1E-02 | 3 | ||||
rs12739262 | 1 | 202422615 | splice region variant | C/T | snv | 1.5E-04 | 7.0E-05 | 3 | |||
rs12751297 | 1 | 242792261 | intergenic variant | G/A | snv | 3 | |||||
rs12978500 | 19 | 406934 | 3 prime UTR variant | C/A | snv | 0.67 | 3 | ||||
rs1573036 | X | 110576840 | intergenic variant | C/T | snv | 0.42 | 3 | ||||
rs1641537 | 17 | 7642403 | upstream gene variant | T/C | snv | 0.75 | 3 | ||||
rs17496332 | 1 | 107003753 | intergenic variant | A/G | snv | 0.26 | 3 | ||||
rs17601876 | 1.000 | 0.080 | 15 | 51261712 | intron variant | A/G | snv | 0.58 | 3 | ||
rs2411984 | 17 | 49368389 | intron variant | G/A | snv | 0.18 | 3 | ||||
rs293428 | 4 | 68726064 | intergenic variant | A/G | snv | 0.36 | 3 | ||||
rs35198051 | 11 | 71134158 | intron variant | G/A | snv | 3 | |||||
rs36019094 | 5 | 40237272 | upstream gene variant | C/A | snv | 3 |