Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17342717 | 6 | 25821542 | intron variant | C/T | snv | 6.1E-02 | 6 | ||||
rs12215823 | 0.925 | 0.120 | 6 | 25725846 | upstream gene variant | G/C;T | snv | 4 | |||
rs1165176 | 0.925 | 0.120 | 6 | 25830070 | intron variant | A/G | snv | 0.65 | 4 | ||
rs1183201 | 0.925 | 0.120 | 6 | 25823216 | intron variant | A/T | snv | 0.65 | 4 | ||
rs12191655 | 0.925 | 0.120 | 6 | 25802867 | intron variant | G/T | snv | 0.14 | 4 | ||
rs1185567 | 0.925 | 0.120 | 6 | 25818360 | intron variant | A/G;T | snv | 4 | |||
rs1165151 | 0.925 | 0.120 | 6 | 25821388 | intron variant | T/A;G | snv | 4 | |||
rs12200962 | 0.925 | 0.120 | 6 | 25828758 | intron variant | T/C | snv | 0.17 | 4 | ||
rs1165215 | 0.882 | 0.200 | 6 | 25798704 | 3 prime UTR variant | G/A | snv | 0.66 | 4 | ||
rs6923367 | 0.925 | 0.120 | 6 | 25745624 | intergenic variant | A/T | snv | 0.26 | 4 | ||
rs2762353 | 0.882 | 0.200 | 6 | 25794203 | intron variant | A/G | snv | 0.66 | 4 | ||
rs1165177 | 0.925 | 0.120 | 6 | 25829431 | intron variant | T/A | snv | 0.65 | 4 | ||
rs1165178 | 0.925 | 0.120 | 6 | 25827288 | intron variant | A/G | snv | 0.65 | 4 | ||
rs3799352 | 0.925 | 0.120 | 6 | 25822392 | intron variant | C/T | snv | 0.65 | 4 | ||
rs1183200 | 0.925 | 0.120 | 6 | 25818418 | intron variant | G/C | snv | 0.66 | 4 | ||
rs3757131 | 0.882 | 0.200 | 6 | 25783681 | intron variant | C/T | snv | 0.32 | 4 | ||
rs1165209 | 0.925 | 0.120 | 6 | 25801091 | intron variant | G/A | snv | 0.66 | 4 | ||
rs3799344 | 0.882 | 0.200 | 6 | 25786765 | intron variant | C/T | snv | 0.41 | 4 | ||
rs765285 | 0.925 | 0.120 | 6 | 25828014 | intron variant | G/C;T | snv | 4 | |||
rs13197601 | 0.882 | 0.200 | 6 | 25785707 | intron variant | G/A | snv | 0.32 | 4 | ||
rs1165153 | 0.925 | 0.120 | 6 | 25817561 | intron variant | A/G;T | snv | 4 | |||
rs1165152 | 0.925 | 0.120 | 6 | 25818538 | intron variant | A/C;G;T | snv | 4 | |||
rs1185569 | 0.925 | 0.120 | 6 | 25831375 | intron variant | A/G | snv | 0.65 | 4 | ||
rs12211184 | 0.925 | 0.120 | 6 | 25823546 | intron variant | G/A | snv | 0.17 | 4 | ||
rs1165196 | 0.882 | 0.200 | 6 | 25812922 | missense variant | G/A | snv | 0.62 | 0.66 | 4 |