Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519719 | 1.000 | 0.080 | 7 | 140781593 | missense variant | T/C | snv | 2 | |||
rs1057520015 | 1.000 | 0.080 | 18 | 20955181 | missense variant | G/A | snv | 2 | |||
rs34158769 | 1.000 | 0.080 | 6 | 26336344 | upstream gene variant | G/A | snv | 8.2E-02 | 2 | ||
rs36162392 | 1.000 | 0.080 | 6 | 26568907 | upstream gene variant | T/A;C;G | snv | 2 | |||
rs4886591 | 1.000 | 0.080 | 15 | 78782176 | intron variant | G/A;C | snv | 2 | |||
rs80264589 | 1.000 | 0.080 | 6 | 26959823 | intron variant | G/A | snv | 7.0E-02 | 2 | ||
rs10436951 | 1.000 | 0.080 | 1 | 243199378 | intron variant | A/G | snv | 7.1E-02 | 1 | ||
rs1057520037 | 1.000 | 0.080 | 7 | 55174782 | missense variant | G/C | snv | 1 | |||
rs11008347 | 1.000 | 0.080 | 10 | 19072094 | intron variant | C/G | snv | 0.12 | 1 | ||
rs114002231 | 1.000 | 0.080 | 6 | 31459618 | intron variant | G/C | snv | 1 | |||
rs114385935 | 1.000 | 0.080 | 6 | 28651576 | upstream gene variant | A/G | snv | 1 | |||
rs114393147 | 1.000 | 0.080 | 6 | 33157965 | downstream gene variant | A/G | snv | 1 | |||
rs114601353 | 1.000 | 0.080 | 6 | 30389517 | intergenic variant | C/T | snv | 1 | |||
rs114828403 | 1.000 | 0.080 | 6 | 32809144 | downstream gene variant | T/C | snv | 1 | |||
rs115100928 | 1.000 | 0.080 | 6 | 32419655 | intergenic variant | G/A | snv | 1 | |||
rs11514963 | 1.000 | 0.080 | 7 | 131247904 | intron variant | C/T | snv | 0.81 | 1 | ||
rs115287935 | 1.000 | 0.080 | 6 | 29006488 | upstream gene variant | G/T | snv | 1 | |||
rs115613607 | 1.000 | 0.080 | 6 | 32413503 | regulatory region variant | G/C | snv | 1 | |||
rs115666025 | 1.000 | 0.080 | 6 | 31009903 | upstream gene variant | G/A | snv | 1 | |||
rs115729734 | 1.000 | 0.080 | 6 | 29931238 | upstream gene variant | T/C;G | snv | 1 | |||
rs115819854 | 1.000 | 0.080 | 6 | 32683864 | intergenic variant | G/T | snv | 1 | |||
rs115870917 | 1.000 | 0.080 | 6 | 29639324 | upstream gene variant | T/C | snv | 1 | |||
rs116165775 | 1.000 | 0.080 | 2 | 67400580 | 3 prime UTR variant | G/A;T | snv | 1 | |||
rs116260619 | 1.000 | 0.080 | 6 | 30479897 | intergenic variant | A/C | snv | 1 | |||
rs116295105 | 1.000 | 0.080 | 6 | 30685004 | missense variant | C/G;T | snv | 1 |