Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs141708090 | 1.000 | 0.120 | 3 | 14761602 | missense variant | G/T | snv | 1.9E-03 | 5.2E-04 | 1 | |
rs2066865 | 0.807 | 0.240 | 4 | 154604124 | downstream gene variant | G/A | snv | 0.26 | 10 | ||
rs936094 | 1.000 | 0.120 | 4 | 158523162 | intron variant | T/A;C;G | snv | 1 | |||
rs4880 | 0.500 | 0.840 | 6 | 159692840 | missense variant | A/G | snv | 0.48 | 0.47 | 131 | |
rs359312 | 1.000 | 0.120 | 10 | 17346144 | intron variant | C/T | snv | 3.6E-02 | 1 | ||
rs34531324 | 1.000 | 0.120 | 5 | 174435441 | intron variant | A/T | snv | 0.16 | 3 | ||
rs1135401746 | 0.827 | 0.400 | 1 | 1806512 | missense variant | C/G | snv | 7 | |||
rs10949482 | 1.000 | 0.120 | 6 | 18121083 | 3 prime UTR variant | C/T | snv | 6.8E-02 | 1 | ||
rs1142345 | 0.776 | 0.280 | 6 | 18130687 | missense variant | T/C;G | snv | 3.7E-02 | 9 | ||
rs79050301 | 1.000 | 0.120 | 6 | 18151959 | intron variant | T/C | snv | 4.5E-02 | 1 | ||
rs2036914 | 0.882 | 0.160 | 4 | 186271327 | intron variant | T/C | snv | 0.57 | 5 | ||
rs17505102 | 1.000 | 0.120 | 3 | 189683987 | intron variant | G/C | snv | 9.7E-02 | 1 | ||
rs920590 | 1.000 | 0.120 | 8 | 19793650 | regulatory region variant | T/C | snv | 0.39 | 3 | ||
rs1569175 | 1.000 | 0.120 | 2 | 200157231 | intergenic variant | T/C | snv | 0.88 | 1 | ||
rs4553808 | 0.672 | 0.320 | 2 | 203866282 | upstream gene variant | A/G;T | snv | 0.16 | 28 | ||
rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 | ||
rs2390536 | 1.000 | 0.120 | 7 | 21445779 | intron variant | G/A | snv | 0.26 | 1 | ||
rs3731217 | 0.763 | 0.320 | 9 | 21984662 | intron variant | A/C;T | snv | 10 | |||
rs2069426 | 1.000 | 0.120 | 9 | 22006274 | intron variant | G/A;C;T | snv | 4.4E-06; 4.4E-06; 7.5E-02 | 1 | ||
rs4266962 | 1.000 | 0.120 | 10 | 22052645 | intergenic variant | C/G;T | snv | 1 | |||
rs4748793 | 0.851 | 0.120 | 10 | 22194082 | intergenic variant | A/G | snv | 0.18 | 4 | ||
rs7901152 | 1.000 | 0.120 | 10 | 22544224 | intron variant | G/A | snv | 0.66 | 1 | ||
rs11013046 | 1.000 | 0.120 | 10 | 22551654 | intron variant | C/T | snv | 0.55 | 1 | ||
rs4748813 | 1.000 | 0.120 | 10 | 22557806 | intron variant | T/A;C | snv | 1 | |||
rs7088318 | 0.851 | 0.120 | 10 | 22564019 | intron variant | C/A | snv | 0.55 | 4 |