Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1165151 | 0.925 | 0.120 | 6 | 25821388 | intron variant | T/A;G | snv | 4 | |||
rs1165152 | 0.925 | 0.120 | 6 | 25818538 | intron variant | A/C;G;T | snv | 4 | |||
rs1165153 | 0.925 | 0.120 | 6 | 25817561 | intron variant | A/G;T | snv | 4 | |||
rs1165176 | 0.925 | 0.120 | 6 | 25830070 | intron variant | A/G | snv | 0.65 | 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 | ||
rs1165196 | 0.882 | 0.200 | 6 | 25812922 | missense variant | G/A | snv | 0.62 | 0.66 | 4 | |
rs1165209 | 0.925 | 0.120 | 6 | 25801091 | intron variant | G/A | snv | 0.66 | 4 | ||
rs1165215 | 0.882 | 0.200 | 6 | 25798704 | 3 prime UTR variant | G/A | snv | 0.66 | 4 | ||
rs1183200 | 0.925 | 0.120 | 6 | 25818418 | intron variant | G/C | snv | 0.66 | 4 | ||
rs1183201 | 0.925 | 0.120 | 6 | 25823216 | intron variant | A/T | snv | 0.65 | 4 | ||
rs1185567 | 0.925 | 0.120 | 6 | 25818360 | intron variant | A/G;T | snv | 4 | |||
rs1185569 | 0.925 | 0.120 | 6 | 25831375 | intron variant | A/G | snv | 0.65 | 4 | ||
rs13197601 | 0.882 | 0.200 | 6 | 25785707 | intron variant | G/A | snv | 0.32 | 4 | ||
rs2762353 | 0.882 | 0.200 | 6 | 25794203 | intron variant | A/G | snv | 0.66 | 4 | ||
rs3757131 | 0.882 | 0.200 | 6 | 25783681 | intron variant | C/T | snv | 0.32 | 4 | ||
rs3799344 | 0.882 | 0.200 | 6 | 25786765 | intron variant | C/T | snv | 0.41 | 4 | ||
rs3799352 | 0.925 | 0.120 | 6 | 25822392 | intron variant | C/T | snv | 0.65 | 4 | ||
rs765285 | 0.925 | 0.120 | 6 | 25828014 | intron variant | G/C;T | snv | 4 | |||
rs11754288 | 0.925 | 0.120 | 6 | 25776721 | missense variant | G/A | snv | 0.36 | 0.32 | 4 | |
rs10498730 | 0.925 | 0.120 | 6 | 25811841 | intron variant | A/G | snv | 3.7E-02 | 3 | ||
rs13200784 | 0.925 | 0.120 | 6 | 25829405 | intron variant | A/T | snv | 0.27 | 3 | ||
rs1324082 | 0.925 | 0.120 | 6 | 25801743 | intron variant | C/T | snv | 0.28 | 3 | ||
rs1408268 | 0.925 | 0.120 | 6 | 25826758 | intron variant | T/A | snv | 0.26 | 3 | ||
rs3799346 | 0.882 | 0.200 | 6 | 25791126 | intron variant | C/T | snv | 0.28 | 3 |