Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs112635299 | 1.000 | 0.040 | 14 | 94371805 | downstream gene variant | G/T | snv | 1.3E-02 | 7 | ||
rs35225200 | 1.000 | 0.040 | 4 | 102225731 | intergenic variant | A/C | snv | 5.4E-02 | 5 | ||
rs1452075 | 1.000 | 0.040 | 3 | 62495388 | intron variant | C/T | snv | 0.73 | 4 | ||
rs4129585 | 1.000 | 0.040 | 8 | 142231572 | intron variant | A/C | snv | 0.68 | 4 | ||
rs6704768 | 1.000 | 0.040 | 2 | 232727791 | intron variant | G/A | snv | 0.54 | 4 | ||
rs6855246 | 1.000 | 0.040 | 4 | 102191313 | intergenic variant | A/G | snv | 0.14 | 4 | ||
rs10149470 | 1.000 | 0.040 | 14 | 103551616 | upstream gene variant | A/G | snv | 0.54 | 3 | ||
rs11210892 | 1.000 | 0.040 | 1 | 43634413 | intergenic variant | G/A | snv | 0.51 | 3 | ||
rs11740474 | 1.000 | 0.040 | 5 | 154301187 | intron variant | A/T | snv | 0.37 | 3 | ||
rs12443170 | 1.000 | 0.040 | 15 | 78615394 | intron variant | G/A | snv | 0.12 | 3 | ||
rs12552 | 1.000 | 0.040 | 13 | 53051646 | 3 prime UTR variant | A/G | snv | 0.58 | 3 | ||
rs12704290 | 1.000 | 0.040 | 7 | 86798310 | intron variant | G/A | snv | 8.9E-02 | 3 | ||
rs12826178 | 1.000 | 0.040 | 12 | 57228588 | upstream gene variant | G/T | snv | 5.3E-02 | 3 | ||
rs133047 | 1.000 | 0.040 | 22 | 40631815 | intron variant | T/C | snv | 0.93 | 3 | ||
rs1620977 | 1.000 | 0.040 | 1 | 72263459 | intron variant | A/G;T | snv | 3 | |||
rs169738 | 1.000 | 0.040 | 6 | 33569769 | intron variant | A/G;T | snv | 3 | |||
rs2535627 | 1.000 | 0.040 | 3 | 52811089 | downstream gene variant | T/A;C;G | snv | 3 | |||
rs3617 | 1.000 | 0.040 | 3 | 52799789 | missense variant | C/A | snv | 0.48 | 0.54 | 3 | |
rs4702 | 1.000 | 0.040 | 15 | 90883330 | 3 prime UTR variant | G/A;C | snv | 3 | |||
rs55661361 | 1.000 | 0.040 | 11 | 124744061 | intron variant | G/A | snv | 0.43 | 3 | ||
rs62378245 | 1.000 | 0.040 | 5 | 89448145 | intron variant | C/T | snv | 0.25 | 3 | ||
rs6940116 | 1.000 | 0.040 | 6 | 27740953 | upstream gene variant | A/G | snv | 0.18 | 3 | ||
rs72986630 | 1.000 | 0.040 | 19 | 11738921 | 5 prime UTR variant | C/A;T | snv | 3 | |||
rs7432375 | 1.000 | 0.040 | 3 | 136569563 | intron variant | G/A | snv | 0.35 | 3 | ||
rs7746199 | 1.000 | 0.040 | 6 | 27293545 | intron variant | C/T | snv | 0.18 | 3 |