Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3764261 | 0.732 | 0.280 | 16 | 56959412 | upstream gene variant | C/A | snv | 0.31 | 11 | ||
rs12678919 | 0.882 | 0.080 | 8 | 19986711 | intergenic variant | A/G | snv | 1.0E-01 | 7 | ||
rs10801551 | 1.000 | 0.040 | 1 | 196610909 | upstream gene variant | G/A;C | snv | 2 | |||
rs10922144 | 1.000 | 0.040 | 1 | 196854170 | intron variant | C/A;T | snv | 2 | |||
rs10922146 | 1.000 | 0.040 | 1 | 196865506 | intron variant | C/T | snv | 0.19 | 2 | ||
rs12029571 | 1.000 | 0.040 | 1 | 196634172 | intergenic variant | A/G | snv | 0.24 | 2 | ||
rs12047098 | 1.000 | 0.040 | 1 | 196865976 | intron variant | T/C | snv | 0.19 | 2 | ||
rs12061508 | 1.000 | 0.040 | 1 | 196615338 | intergenic variant | G/A | snv | 0.23 | 2 | ||
rs1963605 | 1.000 | 0.040 | 1 | 196853038 | intron variant | C/A;T | snv | 2 | |||
rs1964645 | 1.000 | 0.040 | 1 | 196852884 | intron variant | T/A;C | snv | 2 | |||
rs4657825 | 1.000 | 0.040 | 1 | 196615191 | intergenic variant | A/G;T | snv | 2 | |||
rs6657442 | 1.000 | 0.040 | 1 | 196868930 | intron variant | T/C | snv | 0.19 | 2 | ||
rs7413265 | 1.000 | 0.040 | 1 | 196870033 | intron variant | G/T | snv | 0.19 | 2 | ||
rs7555070 | 1.000 | 0.040 | 1 | 197013024 | downstream gene variant | C/T | snv | 0.57 | 2 | ||
rs1021636 | 1.000 | 0.040 | 1 | 196876143 | intron variant | A/G | snv | 0.21 | 1 | ||
rs10510109 | 1.000 | 0.040 | 10 | 122360941 | intergenic variant | G/A;T | snv | 1 | |||
rs10754206 | 1.000 | 0.040 | 1 | 196851794 | intron variant | T/G | snv | 0.41 | 1 | ||
rs10801575 | 1.000 | 0.040 | 1 | 196883651 | intron variant | T/A;C | snv | 1 | |||
rs10887142 | 1.000 | 0.040 | 10 | 122347969 | downstream gene variant | G/A;C | snv | 1 | |||
rs11200576 | 1.000 | 0.040 | 10 | 122358034 | intergenic variant | A/T | snv | 0.13 | 1 | ||
rs11200583 | 1.000 | 0.040 | 10 | 122363954 | regulatory region variant | A/C | snv | 0.13 | 1 | ||
rs12240143 | 1.000 | 0.040 | 1 | 196875887 | intron variant | T/C | snv | 0.39 | 1 | ||
rs12240148 | 1.000 | 0.040 | 1 | 196876177 | intron variant | T/A;C | snv | 1 | |||
rs1332666 | 1.000 | 0.040 | 1 | 197015549 | intergenic variant | A/G;T | snv | 1 | |||
rs13374399 | 1.000 | 0.040 | 1 | 196872876 | intron variant | G/A | snv | 0.22 | 1 |