Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2234693 | 0.555 | 0.680 | 6 | 151842200 | intron variant | T/C | snv | 0.47 | 77 | ||
rs9340799 | 0.583 | 0.680 | 6 | 151842246 | intron variant | A/G | snv | 0.32 | 62 | ||
rs1801132 | 0.689 | 0.320 | 6 | 151944387 | synonymous variant | G/C | snv | 0.73 | 0.80 | 22 | |
rs2077647 | 0.732 | 0.320 | 6 | 151807942 | synonymous variant | T/A;C | snv | 8.1E-06; 0.46 | 16 | ||
rs3798577 | 0.742 | 0.320 | 6 | 152099995 | 3 prime UTR variant | T/C | snv | 0.45 | 16 | ||
rs2228480 | 0.724 | 0.360 | 6 | 152098960 | synonymous variant | G/A | snv | 0.19 | 0.18 | 16 | |
rs796065354 | 0.882 | 0.080 | 6 | 151944320 | missense variant | A/G | snv | 9 | |||
rs762292600 | 0.925 | 0.080 | 6 | 151944316 | missense variant | A/G | snv | 4.0E-06 | 1.4E-05 | 7 | |
rs3020314 | 0.790 | 0.280 | 6 | 151949537 | intron variant | C/G;T | snv | 7 | |||
rs200960801 | 0.827 | 0.200 | 6 | 151944488 | missense variant | A/G | snv | 4.0E-06 | 6 | ||
rs188957694 | 0.882 | 0.080 | 6 | 151944218 | missense variant | G/A;C | snv | 4.0E-05 | 4.9E-05 | 6 | |
rs757200716 | 0.851 | 0.160 | 6 | 151842617 | missense variant | G/A | snv | 8.0E-06 | 5 | ||
rs2273206 | 0.851 | 0.280 | 6 | 152061176 | intron variant | G/T | snv | 0.17 | 0.22 | 5 | |
rs9383938 | 0.827 | 0.160 | 6 | 151666222 | intron variant | G/T | snv | 0.11 | 5 | ||
rs1462893414 | 0.882 | 0.080 | 6 | 151944323 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 5 | |
rs2881766 | 0.882 | 0.120 | 6 | 151797984 | intron variant | T/G | snv | 0.35 | 5 | ||
rs904571820 | 0.851 | 0.160 | 6 | 151842664 | start lost | A/G | snv | 4.0E-06 | 5 | ||
rs2144025 | 0.925 | 0.080 | 6 | 151986571 | intron variant | T/A;C | snv | 4 | |||
rs200075329 | 0.925 | 0.080 | 6 | 151808264 | missense variant | T/C | snv | 4.4E-03 | 4.3E-03 | 4 | |
rs200282497 | 0.925 | 0.080 | 6 | 151944239 | missense variant | G/C | snv | 3.6E-05 | 3.5E-05 | 4 | |
rs1364963022 | 0.925 | 0.080 | 6 | 151944233 | missense variant | G/C | snv | 4.0E-06 | 4 | ||
rs1062577 | 0.882 | 0.080 | 6 | 152102770 | 3 prime UTR variant | T/A;G | snv | 4 | |||
rs746432 | 0.851 | 0.120 | 6 | 151808173 | synonymous variant | G/A;C | snv | 6.6E-02 | 7.0E-02 | 4 | |
rs149308960 | 0.925 | 0.080 | 6 | 151842622 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06; 1.6E-03 | 4 | ||
rs1884051 | 0.882 | 0.080 | 6 | 151962144 | intron variant | G/A | snv | 0.60 | 4 |