Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4444235 | 0.701 | 0.240 | 14 | 53944201 | downstream gene variant | T/C | snv | 0.43 | 23 | ||
rs12229654 | 0.763 | 0.320 | 12 | 110976657 | intergenic variant | T/G | snv | 4.8E-03 | 20 | ||
rs1321311 | 0.742 | 0.160 | 6 | 36655123 | regulatory region variant | C/A | snv | 0.28 | 15 | ||
rs10484761 | 0.807 | 0.080 | 6 | 40834522 | intergenic variant | T/C | snv | 0.31 | 7 | ||
rs31563 | 0.851 | 0.160 | 5 | 135899917 | intron variant | C/A;T | snv | 5 | |||
rs312986 | 0.925 | 0.080 | 18 | 1898710 | intron variant | A/G;T | snv | 3 | |||
rs6772209 | 1.000 | 0.080 | 3 | 175929377 | intergenic variant | G/A | snv | 4.1E-02 | 2 | ||
rs8030672 | 1.000 | 0.080 | 15 | 68766745 | intergenic variant | T/A | snv | 5.4E-02 | 2 | ||
rs10002268 | 1.000 | 0.080 | 4 | 55653725 | intergenic variant | T/C | snv | 0.41 | 1 | ||
rs12542990 | 1.000 | 0.080 | 8 | 81122216 | intergenic variant | G/C | snv | 0.32 | 1 | ||
rs17028375 | 1.000 | 0.080 | 2 | 64085008 | downstream gene variant | T/C | snv | 0.11 | 1 | ||
rs6123557 | 1.000 | 0.080 | 20 | 56232196 | intergenic variant | C/T | snv | 0.21 | 1 | ||
rs7726463 | 1.000 | 0.080 | 5 | 37954971 | intron variant | T/C | snv | 9.1E-02 | 1 | ||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs748676559 | 0.925 | 0.080 | 17 | 37284932 | missense variant | C/T | snv | 4.0E-06 | 2.1E-05 | 3 | |
rs11066015 | 0.925 | 0.120 | 12 | 111730205 | intron variant | G/A | snv | 5.9E-03 | 5 | ||
rs11066008 | 1.000 | 0.080 | 12 | 111702865 | intron variant | A/G | snv | 9.1E-03 | 1 | ||
rs1800682 | 0.637 | 0.440 | 10 | 88990206 | non coding transcript exon variant | A/G | snv | 0.54 | 32 | ||
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 83 | ||
rs698 | 0.724 | 0.240 | 4 | 99339632 | missense variant | T/A;C | snv | 0.35 | 20 | ||
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
rs201745983 | 0.752 | 0.200 | 12 | 111783219 | missense variant | G/A | snv | 6.8E-05 | 7.7E-05 | 14 | |
rs4646776 | 0.925 | 0.120 | 12 | 111792215 | intron variant | G/A;C | snv | 1.9E-02 | 5.8E-03 | 2 | |
rs1801155 | 0.649 | 0.440 | 5 | 112839514 | missense variant | T/A | snv | 8.0E-06; 2.0E-03 | 1.2E-03 | 42 | |
rs1463038513 | 0.658 | 0.440 | 5 | 112839511 | frameshift variant | TAAA/- | delins | 36 |