Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11088680 | 0.925 | 0.080 | 21 | 13514758 | upstream gene variant | A/G | snv | 0.30 | 2 | ||
rs1887427 | 0.925 | 0.080 | 9 | 4979730 | upstream gene variant | A/G | snv | 0.21 | 2 | ||
rs1892901 | 0.925 | 0.080 | 11 | 65903422 | upstream gene variant | G/A | snv | 9.5E-03 | 2 | ||
rs26160 | 0.925 | 0.080 | 5 | 145353893 | intron variant | T/C | snv | 4.5E-03 | 2 | ||
rs36012910 | 0.925 | 0.080 | 2 | 25345310 | upstream gene variant | A/C;G | snv | 2 | |||
rs4145643 | 0.925 | 0.080 | 10 | 60803097 | regulatory region variant | G/C;T | snv | 2 | |||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
rs1305398818 | 0.925 | 0.080 | 4 | 88131886 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 | 4 | ||
rs505922 | 0.689 | 0.520 | 9 | 133273813 | intron variant | C/T | snv | 34 | |||
rs6713088 | 0.763 | 0.200 | 2 | 54118332 | intron variant | C/G | snv | 0.48 | 9 | ||
rs11896604 | 0.776 | 0.200 | 2 | 54252062 | intron variant | C/A;G;T | snv | 8 | |||
rs843706 | 0.807 | 0.160 | 2 | 54253232 | 3 prime UTR variant | C/A | snv | 0.42 | 6 | ||
rs4963 | 0.827 | 0.120 | 4 | 2915035 | missense variant | C/G;T | snv | 0.20 | 0.18 | 6 | |
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 83 | ||
rs17033 | 0.925 | 0.080 | 4 | 99307788 | 3 prime UTR variant | T/C | snv | 9.6E-02 | 3 | ||
rs283411 | 0.925 | 0.080 | 4 | 99344800 | intron variant | C/A;T | snv | 2 | |||
rs266729 | 0.637 | 0.560 | 3 | 186841685 | upstream gene variant | C/A;G;T | snv | 37 | |||
rs822395 | 0.776 | 0.240 | 3 | 186849018 | intron variant | C/A;G | snv | 10 | |||
rs12733285 | 0.776 | 0.120 | 1 | 202952912 | intron variant | C/T | snv | 0.26 | 12 | ||
rs1342387 | 0.776 | 0.120 | 1 | 202945228 | intron variant | T/C | snv | 0.53 | 12 | ||
rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 82 | |
rs184003 | 0.724 | 0.400 | 6 | 32182519 | intron variant | C/A | snv | 0.12 | 0.12 | 15 | |
rs1800625 | 0.641 | 0.680 | 6 | 32184665 | upstream gene variant | A/G | snv | 0.15 | 39 | ||
rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 134 |