Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 24 | ||
rs657152 | 0.882 | 0.200 | 9 | 133263862 | intron variant | A/C;T | snv | 14 | |||
rs651007 | 0.851 | 0.160 | 9 | 133278431 | upstream gene variant | T/A;C | snv | 11 | |||
rs673548 | 0.925 | 0.120 | 2 | 21014672 | intron variant | G/A;T | snv | 10 | |||
rs1532085 | 0.882 | 0.080 | 15 | 58391167 | intron variant | A/G;T | snv | 9 | |||
rs174548 | 0.851 | 0.160 | 11 | 61803876 | 5 prime UTR variant | C/G;T | snv | 9 | |||
rs174576 | 0.851 | 0.200 | 11 | 61836038 | intron variant | C/A;T | snv | 9 | |||
rs599839 | 0.724 | 0.360 | 1 | 109279544 | downstream gene variant | G/A;C | snv | 9 | |||
rs630014 | 9 | 133274306 | intron variant | G/A;C | snv | 9 | |||||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 8 | ||
rs174601 | 0.925 | 0.080 | 11 | 61855668 | non coding transcript exon variant | C/A;T | snv | 8 | |||
rs649129 | 1.000 | 0.080 | 9 | 133278860 | upstream gene variant | T/C;G | snv | 8 | |||
rs11206510 | 0.763 | 0.240 | 1 | 55030366 | intergenic variant | T/A;C;G | snv | 7 | |||
rs1800775 | 0.790 | 0.240 | 16 | 56961324 | upstream gene variant | C/A;G | snv | 0.51; 5.7E-06 | 7 | ||
rs2075290 | 0.882 | 0.160 | 11 | 116782580 | intron variant | C/G;T | snv | 7 | |||
rs2516448 | 0.827 | 0.120 | 6 | 31422633 | intron variant | T/C;G | snv | 7 | |||
rs635634 | 0.882 | 0.160 | 9 | 133279427 | upstream gene variant | T/A;C | snv | 7 | |||
rs6589566 | 0.882 | 0.080 | 11 | 116781707 | intron variant | G/A;C;T | snv | 7 | |||
rs676210 | 0.925 | 0.120 | 2 | 21008652 | missense variant | G/A;T | snv | 0.29 | 7 | ||
rs11570255 | 1.000 | 20 | 59300861 | missense variant | G/A;T | snv | 3.3E-03; 2.9E-05 | 6 | |||
rs11571151 | 11 | 101127486 | missense variant | C/G;T | snv | 6 | |||||
rs1169288 | 0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 | 6 | ||
rs17240378 | 16 | 67942790 | intron variant | G/C;T | snv | 4.0E-06 | 6 | ||||
rs1800588 | 0.790 | 0.200 | 15 | 58431476 | intron variant | C/G;T | snv | 0.30 | 6 | ||
rs2001945 | 8 | 125465736 | upstream gene variant | G/A;C;T | snv | 6 |