Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12576775 | 0.827 | 0.080 | 11 | 79366149 | intron variant | A/G | snv | 0.15 | 2 | ||
rs1511237 | 1.000 | 0.040 | 11 | 79403640 | intron variant | C/T | snv | 0.11 | 1 | ||
rs1944449 | 1.000 | 0.040 | 11 | 79372205 | intron variant | C/T | snv | 0.18 | 1 | ||
rs11237799 | 1.000 | 0.040 | 11 | 79356427 | intron variant | A/C;T | snv | 1 | |||
rs10501439 | 1.000 | 0.040 | 11 | 79374802 | intron variant | A/G | snv | 0.18 | 1 | ||
rs11237815 | 1.000 | 0.040 | 11 | 79379756 | intron variant | A/G | snv | 0.10 | 1 | ||
rs12577328 | 1.000 | 0.040 | 11 | 79382430 | intron variant | C/G | snv | 8.3E-02 | 1 | ||
rs11237821 | 1.000 | 0.040 | 11 | 79395760 | intron variant | C/A;T | snv | 1 | |||
rs12577093 | 1.000 | 0.040 | 11 | 79346052 | intron variant | C/A;T | snv | 1 | |||
rs7108878 | 1.000 | 0.040 | 11 | 79396763 | intron variant | T/G | snv | 0.10 | 1 | ||
rs17138230 | 0.925 | 0.080 | 11 | 79364808 | intron variant | A/T | snv | 0.16 | 1 | ||
rs11237805 | 1.000 | 0.040 | 11 | 79367625 | intron variant | A/G;T | snv | 1 | |||
rs12275195 | 1.000 | 0.040 | 11 | 79394755 | intron variant | A/C | snv | 0.12 | 1 | ||
rs12290811 | 0.882 | 0.120 | 11 | 79372576 | intron variant | T/A | snv | 0.18 | 1 | ||
rs12277834 | 1.000 | 0.040 | 11 | 79389112 | intron variant | C/A;T | snv | 1 | |||
rs17138171 | 1.000 | 0.040 | 11 | 79351885 | intron variant | T/A;C | snv | 1 | |||
rs7127580 | 1.000 | 0.040 | 11 | 79433812 | intron variant | C/A;G | snv | 1 | |||
rs12289486 | 1.000 | 0.040 | 11 | 79381483 | intron variant | C/T | snv | 8.4E-02 | 1 | ||
rs11237796 | 1.000 | 0.040 | 11 | 79348399 | intron variant | A/G | snv | 0.16 | 1 | ||
rs954129 | 1.000 | 0.040 | 11 | 79349751 | intron variant | T/A | snv | 0.18 | 1 | ||
rs12279388 | 1.000 | 0.040 | 11 | 79356629 | intron variant | A/G | snv | 0.15 | 1 | ||
rs11237820 | 1.000 | 0.040 | 11 | 79393621 | intron variant | G/A | snv | 8.7E-02 | 1 | ||
rs7932890 | 0.925 | 0.080 | 11 | 79357349 | intron variant | A/G | snv | 0.19 | 1 | ||
rs499949 | 11 | 79282162 | intron variant | C/T | snv | 0.58 | 1 | ||||
rs1151200 | 11 | 79281641 | intron variant | T/C | snv | 0.50 | 1 |