Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2284378 | 0.851 | 0.080 | 20 | 34000289 | intron variant | T/C;G | snv | 4 | |||
rs559848002 | 0.925 | 0.120 | 9 | 21971147 | missense variant | T/C;G | snv | 4.7E-06 | 3 | ||
rs62068372 | 0.925 | 0.080 | 16 | 89718699 | intron variant | T/C;G | snv | 2 | |||
rs6431588 | 0.925 | 0.040 | 2 | 238185147 | intron variant | T/C;G | snv | 0.86 | 0.85 | 2 | |
rs7033503 | 1.000 | 0.040 | 9 | 21799599 | upstream gene variant | T/C;G | snv | 1 | |||
rs77064436 | 1.000 | 0.040 | 3 | 41224577 | missense variant | T/C;G | snv | 1 | |||
rs25487 | 0.441 | 0.800 | 19 | 43551574 | missense variant | T/C | snv | 0.68 | 0.71 | 205 | |
rs758272654 | 0.611 | 0.680 | 20 | 58909201 | synonymous variant | T/C | snv | 4.0E-06 | 7.0E-06 | 50 | |
rs121913513 | 0.776 | 0.120 | 4 | 54727495 | missense variant | T/C | snv | 10 | |||
rs4516035 | 0.776 | 0.360 | 12 | 47906043 | non coding transcript exon variant | T/C | snv | 0.31 | 10 | ||
rs2036534 | 0.827 | 0.080 | 15 | 78534606 | 3 prime UTR variant | T/C | snv | 0.26 | 8 | ||
rs10931936 | 0.827 | 0.120 | 2 | 201279205 | intron variant | T/C | snv | 0.72 | 6 | ||
rs1512268 | 0.851 | 0.160 | 8 | 23668950 | intergenic variant | T/C | snv | 0.50 | 6 | ||
rs587779826 | 0.851 | 0.360 | 11 | 108267344 | splice donor variant | T/C | snv | 4.0E-06 | 5 | ||
rs6914598 | 0.851 | 0.080 | 6 | 21163688 | intron variant | T/C | snv | 0.38 | 4 | ||
rs1057519805 | 1.000 | 0.040 | 15 | 66436839 | missense variant | T/C | snv | 3 | |||
rs1057519806 | 0.882 | 0.200 | 19 | 4110583 | missense variant | T/C | snv | 3 | |||
rs1110400 | 1.000 | 0.040 | 16 | 89919722 | missense variant | T/C | snv | 5.6E-03 | 6.6E-03 | 3 | |
rs12512631 | 0.882 | 0.200 | 4 | 71735614 | intergenic variant | T/C | snv | 0.35 | 3 | ||
rs766310650 | 1.000 | 0.040 | 6 | 36677906 | 5 prime UTR variant | T/C | snv | 6.2E-05 | 2.1E-05 | 3 | |
rs1057519702 | 1.000 | 0.040 | 4 | 54726020 | missense variant | T/C | snv | 2 | |||
rs1487774219 | 1.000 | 0.040 | 9 | 22008910 | missense variant | T/C | snv | 8.1E-06 | 2 | ||
rs542002959 | 0.925 | 0.120 | 17 | 5558937 | missense variant | T/C | snv | 4.0E-06 | 1.4E-05 | 2 | |
rs1051849 | 1.000 | 0.040 | 17 | 37513222 | 3 prime UTR variant | T/C | snv | 9.9E-02 | 1 | ||
rs1057519812 | 1.000 | 0.040 | 4 | 54277977 | missense variant | T/C | snv | 1 |