Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 25 | |
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 14 | |
rs8050136 | 0.716 | 0.560 | 16 | 53782363 | intron variant | C/A | snv | 0.40 | 11 | ||
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 10 | |
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 10 | ||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 8 | ||
rs3782886 | 0.724 | 0.480 | 12 | 111672685 | synonymous variant | T/C | snv | 1.9E-02 | 5.9E-03 | 7 | |
rs1421085 | 0.752 | 0.280 | 16 | 53767042 | intron variant | T/C | snv | 0.31 | 7 | ||
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 6 | ||
rs17817449 | 0.716 | 0.560 | 16 | 53779455 | intron variant | T/A;G | snv | 5 | |||
rs738409 | 0.557 | 0.720 | 22 | 43928847 | missense variant | C/G | snv | 0.28 | 0.22 | 5 | |
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 4 | |
rs578776 | 0.742 | 0.240 | 15 | 78596058 | 3 prime UTR variant | G/A | snv | 0.39 | 3 | ||
rs2239803 | 0.882 | 0.240 | 6 | 32444056 | intron variant | C/A;T | snv | 0.50 | 3 | ||
rs10483038 | 1.000 | 0.080 | 21 | 37652469 | intron variant | T/C | snv | 0.26 | 3 | ||
rs111372083 | 1.000 | 0.080 | 21 | 37638374 | intron variant | C/A;T | snv | 0.27 | 3 | ||
rs111576572 | 1.000 | 0.080 | 21 | 37617262 | 3 prime UTR variant | A/G | snv | 0.32 | 3 | ||
rs1399590 | 1.000 | 0.080 | 21 | 37681768 | intron variant | G/A | snv | 0.56 | 3 | ||
rs1399591 | 1.000 | 0.080 | 21 | 37681654 | intron variant | C/T | snv | 0.50 | 3 | ||
rs1399592 | 1.000 | 0.080 | 21 | 37681559 | intron variant | T/A;G | snv | 0.52 | 3 | ||
rs1475839 | 1.000 | 0.080 | 21 | 37649639 | intron variant | C/T | snv | 0.31 | 3 | ||
rs1515050 | 1.000 | 0.080 | 21 | 37630840 | intron variant | T/C | snv | 0.75 | 3 | ||
rs1709817 | 1.000 | 0.080 | 21 | 37664047 | intron variant | T/A;C | snv | 3 | |||
rs1709818 | 1.000 | 0.080 | 21 | 37663909 | intron variant | T/C | snv | 0.57 | 3 | ||
rs1709819 | 1.000 | 0.080 | 21 | 37663813 | intron variant | A/C | snv | 0.59 | 3 |