Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17789218 | 6 | 100152221 | intergenic variant | T/A;C | snv | 3 | |||||
rs9496567 | 6 | 100154877 | intergenic variant | G/A | snv | 0.24 | 2 | ||||
rs7955221 | 12 | 100456972 | intergenic variant | A/C;T | snv | 2 | |||||
rs75061399 | 12 | 100548299 | intron variant | G/A | snv | 2.2E-02 | 1 | ||||
rs221797 | 7 | 100688351 | 5 prime UTR variant | A/C;T | snv | 1 | |||||
rs10185855 | 2 | 101025798 | intron variant | A/G | snv | 0.35 | 4 | ||||
rs17199964 | 4 | 101786634 | intron variant | G/A;C | snv | 5 | |||||
rs10275712 | 7 | 1043282 | intron variant | G/A | snv | 0.18 | 1 | ||||
rs2853579 | 9 | 104828991 | synonymous variant | G/T | snv | 0.20 | 0.23 | 3 | |||
rs7873387 | 9 | 104833321 | intron variant | A/C | snv | 0.20 | 1 | ||||
rs12686004 | 1.000 | 0.040 | 9 | 104891145 | intron variant | G/A | snv | 9.1E-02 | 5 | ||
rs2740488 | 0.827 | 0.120 | 9 | 104899461 | intron variant | A/C | snv | 0.29 | 9 | ||
rs1883025 | 0.807 | 0.120 | 9 | 104902020 | intron variant | C/T | snv | 0.28 | 6 | ||
rs2575876 | 9 | 104903458 | intron variant | G/A | snv | 0.24 | 6 | ||||
rs1800978 | 1.000 | 0.040 | 9 | 104903697 | 5 prime UTR variant | C/A;G;T | snv | 5.4E-06; 0.14 | 6 | ||
rs648324 | 1 | 10496390 | intron variant | G/C;T | snv | 2 | |||||
rs62128801 | 19 | 10558487 | intron variant | G/A;C | snv | 2 | |||||
rs7821092 | 8 | 10651291 | intron variant | G/C | snv | 0.54 | 1 | ||||
rs1730859 | 1 | 107075085 | intergenic variant | G/A | snv | 0.75 | 2 | ||||
rs11671653 | 1.000 | 0.040 | 19 | 10727810 | intron variant | G/A;T | snv | 1 | |||
rs2712199 | 7 | 107499794 | intron variant | A/G | snv | 0.29 | 1 | ||||
rs1610095 | 19 | 10794013 | intron variant | G/A;C | snv | 2 | |||||
rs826681 | 2 | 108615619 | intron variant | C/T | snv | 0.17 | 2 | ||||
rs826682 | 2 | 108615932 | intron variant | A/C | snv | 0.18 | 1 | ||||
rs3741782 | 1.000 | 0.040 | 12 | 108701361 | intron variant | A/G;T | snv | 0.31; 4.0E-06 | 2 |