Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3740753 | 0.925 | 0.080 | 11 | 101128040 | missense variant | C/G | snv | 0.13 | 0.12 | 2 | |
rs1408080623 | 0.851 | 0.080 | 11 | 101128058 | missense variant | G/A | snv | 5 | |||
rs776880789 | 0.925 | 0.080 | 11 | 101128241 | missense variant | G/C;T | snv | 4.7E-06; 4.7E-06 | 4 | ||
rs761872690 | 0.925 | 0.080 | 11 | 101128246 | synonymous variant | G/A | snv | 2.8E-05 | 3 | ||
rs750042441 | 0.827 | 0.160 | 11 | 101128367 | missense variant | G/A;C | snv | 6.1E-05; 4.3E-06 | 5 | ||
rs1312187959 | 0.925 | 0.080 | 11 | 101128554 | missense variant | C/T | snv | 1.4E-05 | 7.0E-06 | 2 | |
rs376101426 | 0.925 | 0.080 | 11 | 101128556 | missense variant | A/G | snv | 1.4E-05 | 2.8E-05 | 2 | |
rs772873062 | 0.925 | 0.080 | 11 | 101128998 | missense variant | A/G | snv | 4.8E-06 | 2 | ||
rs757679709 | 0.925 | 0.080 | 11 | 101129045 | missense variant | G/A;C | snv | 3.0E-05 | 2 | ||
rs10895068 | 0.752 | 0.240 | 11 | 101129483 | 5 prime UTR variant | C/T | snv | 3.6E-02 | 14 | ||
rs518162 | 0.925 | 0.080 | 11 | 101129770 | 5 prime UTR variant | A/G | snv | 0.86 | 2 | ||
rs763351020 | 0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 | 35 | ||
rs9874 | 0.925 | 0.080 | 15 | 101271199 | 3 prime UTR variant | T/C | snv | 0.23 | 2 | ||
rs763258401 | 1.000 | 0.080 | 2 | 101308570 | stop gained | C/A;T | snv | 6.0E-06 | 1 | ||
rs2850328 | 0.925 | 0.080 | 4 | 101347783 | non coding transcript exon variant | T/C;G | snv | 2 | |||
rs140657361 | 1.000 | 0.080 | 12 | 101352104 | missense variant | A/T | snv | 3.4E-04 | 1.5E-03 | 1 | |
rs61697963 | 0.925 | 0.080 | 3 | 101458800 | intron variant | A/C;G | snv | 2 | |||
rs16405 | 0.882 | 0.120 | 10 | 101553963 | 3 prime UTR variant | AACAGTGGA/- | del | 0.31 | 4 | ||
rs2228611 | 0.708 | 0.520 | 19 | 10156401 | synonymous variant | T/A;C | snv | 0.52 | 19 | ||
rs3730477 | 0.925 | 0.080 | 10 | 101580299 | missense variant | G/A | snv | 0.17 | 0.16 | 4 | |
rs16999593 | 0.742 | 0.240 | 19 | 10180505 | missense variant | T/C | snv | 2.4E-02 | 9.6E-03 | 14 | |
rs10490571 | 0.827 | 0.320 | 2 | 102100877 | intron variant | C/T | snv | 0.29 | 5 | ||
rs1820453 | 0.925 | 0.080 | 11 | 102109604 | non coding transcript exon variant | C/A | snv | 0.54 | 2 | ||
rs61746398 | 0.925 | 0.080 | 11 | 102205922 | missense variant | C/T | snv | 5.4E-04 | 7.0E-04 | 2 | |
rs1416580204 | 0.608 | 0.720 | 14 | 102250837 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 49 |