Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 24 | ||
rs34811474 | 1.000 | 0.040 | 4 | 25407216 | missense variant | G/A;T | snv | 0.15; 4.1E-06 | 8 | ||
rs17199964 | 4 | 101786634 | intron variant | G/A;C | snv | 5 | |||||
rs177430 | 18 | 23506161 | intron variant | C/A;T | snv | 4 | |||||
rs8089865 | 1.000 | 0.040 | 18 | 53431552 | intron variant | G/A;C | snv | 4 | |||
rs10010325 | 1.000 | 0.040 | 4 | 105185196 | intron variant | C/A;G;T | snv | 3 | |||
rs13262595 | 1.000 | 0.040 | 8 | 142235609 | intron variant | A/C;G | snv | 3 | |||
rs1541374 | 4 | 105127203 | intergenic variant | T/A;G | snv | 3 | |||||
rs1620977 | 1.000 | 0.040 | 1 | 72263459 | intron variant | A/G;T | snv | 3 | |||
rs2302190 | 17 | 58507147 | missense variant | T/A;C | snv | 0.24 | 3 | ||||
rs268134 | 0.925 | 0.120 | 2 | 65381229 | intron variant | A/C;G;T | snv | 3 | |||
rs3747631 | 1.000 | 0.040 | 1 | 204618441 | missense variant | G/A;C | snv | 4.0E-06; 0.20 | 3 | ||
rs3843954 | 1.000 | 0.040 | 13 | 57974377 | intergenic variant | G/A;C | snv | 3 | |||
rs4664442 | 1.000 | 0.040 | 2 | 161971491 | intron variant | G/A;C | snv | 3 | |||
rs4702 | 1.000 | 0.040 | 15 | 90883330 | 3 prime UTR variant | G/A;C | snv | 3 | |||
rs6712515 | 0.925 | 0.160 | 2 | 100190052 | intron variant | T/A;C | snv | 3 | |||
rs72986630 | 1.000 | 0.040 | 19 | 11738921 | 5 prime UTR variant | C/A;T | snv | 3 | |||
rs7924036 | 10 | 63431885 | intron variant | G/A;T | snv | 3 | |||||
rs8049439 | 0.925 | 0.120 | 16 | 28826194 | intron variant | T/C;G | snv | 0.38 | 3 | ||
rs9556958 | 1.000 | 0.040 | 13 | 98447792 | 3 prime UTR variant | C/G;T | snv | 3 | |||
rs9636107 | 1.000 | 0.040 | 18 | 55532886 | intron variant | A/G;T | snv | 3 | |||
rs9906944 | 17 | 49014058 | intron variant | C/G;T | snv | 3 | |||||
rs10061788 | 1.000 | 0.040 | 5 | 88638889 | intron variant | G/A;T | snv | 2 | |||
rs10757417 | 1.000 | 0.040 | 9 | 23347855 | intron variant | G/A;T | snv | 2 | |||
rs1076884 | 1.000 | 0.040 | 16 | 13653946 | intergenic variant | C/G;T | snv | 2 |