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 | 61 | ||
rs79105258 | 12 | 111280427 | intron variant | C/A;T | snv | 23 | |||||
rs28929474 | 0.708 | 0.320 | 14 | 94378610 | missense variant | C/G;T | snv | 2.8E-05; 1.1E-02 | 17 | ||
rs635634 | 0.882 | 0.160 | 9 | 133279427 | upstream gene variant | T/A;C | snv | 17 | |||
rs855791 | 0.701 | 0.400 | 22 | 37066896 | missense variant | A/G;T | snv | 0.57; 4.0E-06 | 17 | ||
rs478442 | 0.851 | 0.120 | 2 | 21176344 | intergenic variant | G/C;T | snv | 16 | |||
rs2519093 | 0.882 | 0.200 | 9 | 133266456 | intron variant | T/C | snv | 14 | |||
rs651007 | 0.851 | 0.160 | 9 | 133278431 | upstream gene variant | T/A;C | snv | 11 | |||
rs1128249 | 1.000 | 0.080 | 2 | 164672114 | intron variant | G/C;T | snv | 9 | |||
rs174548 | 0.851 | 0.160 | 11 | 61803876 | 5 prime UTR variant | C/G;T | snv | 9 | |||
rs1169288 | 0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 | 8 | ||
rs17231506 | 0.851 | 0.040 | 16 | 56960616 | upstream gene variant | C/G;T | snv | 0.28 | 8 | ||
rs13108218 | 4 | 3442204 | intron variant | A/G;T | snv | 7 | |||||
rs174601 | 0.925 | 0.080 | 11 | 61855668 | non coding transcript exon variant | C/A;T | snv | 7 | |||
rs2001945 | 8 | 125465736 | upstream gene variant | G/A;C;T | snv | 7 | |||||
rs550057 | 0.925 | 0.080 | 9 | 133271182 | intron variant | T/A;C | snv | 7 | |||
rs673548 | 0.925 | 0.120 | 2 | 21014672 | intron variant | G/A;T | snv | 7 | |||
rs11591147 | 0.677 | 0.360 | 1 | 55039974 | missense variant | G/A;T | snv | 1.2E-02 | 6 | ||
rs1800978 | 1.000 | 0.040 | 9 | 104903697 | 5 prime UTR variant | C/A;G;T | snv | 5.4E-06; 0.14 | 6 | ||
rs4299376 | 0.851 | 0.120 | 2 | 43845437 | intron variant | G/C;T | snv | 6 | |||
rs507666 | 1.000 | 0.040 | 9 | 133273983 | intron variant | A/G | snv | 6 | |||
rs599839 | 0.724 | 0.360 | 1 | 109279544 | downstream gene variant | G/A;C | snv | 6 | |||
rs127430 | 20 | 58589799 | intron variant | A/G;T | snv | 5 | |||||
rs17199964 | 4 | 101786634 | intron variant | G/A;C | snv | 5 | |||||
rs1801689 | 17 | 66214462 | missense variant | A/C;G | snv | 4.0E-06; 2.4E-02; 4.8E-05 | 5 |