Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3792785 | 1.000 | 0.120 | 5 | 151072089 | intron variant | T/C | snv | 0.13 | 1 | ||
rs3130473 | 0.882 | 0.160 | 6 | 31231431 | intergenic variant | C/T | snv | 0.23 | 6 | ||
rs2524005 | 0.882 | 0.160 | 6 | 29931900 | upstream gene variant | G/A | snv | 0.18 | 3 | ||
rs1422673 | 0.925 | 0.160 | 5 | 151059427 | intron variant | C/G;T | snv | 2 | |||
rs1634718 | 0.925 | 0.160 | 6 | 31005088 | regulatory region variant | A/G | snv | 0.20 | 2 | ||
rs2233287 | 0.925 | 0.160 | 5 | 151060536 | intron variant | G/A | snv | 0.11 | 2 | ||
rs886403 | 0.925 | 0.160 | 6 | 30989841 | 3 prime UTR variant | T/C | snv | 0.23 | 2 | ||
rs9270986 | 0.882 | 0.160 | 6 | 32606283 | intergenic variant | A/C | snv | 0.85 | 2 | ||
rs2071591 | 0.925 | 0.160 | 6 | 31548022 | intron variant | G/A;C | snv | 1 | |||
rs4678 | 0.925 | 0.200 | 6 | 30926164 | missense variant | G/A | snv | 0.14 | 0.15 | 2 | |
rs887464 | 0.925 | 0.200 | 6 | 31178143 | intron variant | C/A;T | snv | 2 | |||
rs7749323 | 0.925 | 0.200 | 6 | 137909252 | intergenic variant | G/A | snv | 3.3E-02 | 1 | ||
rs2844657 | 0.882 | 0.240 | 6 | 30861745 | upstream gene variant | A/G | snv | 0.17 | 3 | ||
rs3095089 | 0.882 | 0.240 | 6 | 30966017 | upstream gene variant | G/T | snv | 0.16 | 3 | ||
rs1265159 | 0.882 | 0.240 | 6 | 31172270 | intron variant | G/A | snv | 0.21 | 2 | ||
rs3130380 | 0.807 | 0.280 | 6 | 30311353 | intron variant | G/A | snv | 6.6E-02 | 10 | ||
rs9261290 | 0.807 | 0.280 | 6 | 30070870 | 3 prime UTR variant | T/C;G | snv | 5.2E-02; 7.2E-06 | 10 | ||
rs11229 | 0.851 | 0.280 | 6 | 31635993 | synonymous variant | A/G | snv | 0.14 | 0.17 | 6 | |
rs1235162 | 0.827 | 0.280 | 6 | 29569447 | intron variant | A/G | snv | 6.0E-02 | 6 | ||
rs2523987 | 0.827 | 0.280 | 6 | 30112216 | intron variant | A/C | snv | 9.2E-02 | 5 | ||
rs3094054 | 0.807 | 0.280 | 6 | 30365728 | upstream gene variant | G/A;T | snv | 5 | |||
rs3129890 | 0.827 | 0.280 | 6 | 32446496 | downstream gene variant | T/A;C | snv | 5 | |||
rs3130350 | 0.827 | 0.280 | 6 | 30360062 | upstream gene variant | G/T | snv | 7.1E-02 | 5 | ||
rs3132610 | 0.807 | 0.280 | 6 | 30576624 | intron variant | A/G | snv | 7.4E-02 | 5 | ||
rs204990 | 0.851 | 0.280 | 6 | 32193653 | intron variant | C/A;T | snv | 4 |