Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6671633 | 1.000 | 0.040 | 1 | 45034622 | intron variant | A/G | snv | 0.59 | 1 | ||
rs6678726 | 1.000 | 0.040 | 1 | 45030723 | intron variant | A/G;T | snv | 1 | |||
rs909406 | 1.000 | 0.040 | 16 | 3099517 | upstream gene variant | C/T | snv | 0.47 | 1 | ||
rs3739028 | 1.000 | 0.040 | 2 | 135150276 | intron variant | T/C | snv | 3.7E-02 | 1 | ||
rs10407807 | 1.000 | 0.040 | 19 | 19935293 | 3 prime UTR variant | C/A | snv | 8.4E-02 | 1 | ||
rs10411195 | 1.000 | 0.040 | 19 | 19925367 | intron variant | T/C | snv | 8.0E-02 | 1 | ||
rs11786 | 1.000 | 0.040 | 19 | 19935409 | 3 prime UTR variant | C/T | snv | 9.3E-02 | 1 | ||
rs12610295 | 1.000 | 0.040 | 19 | 19928158 | intron variant | C/A | snv | 0.15 | 1 | ||
rs2335367 | 1.000 | 0.040 | 19 | 19913057 | intron variant | T/C | snv | 0.96 | 1 | ||
rs4809014 | 1.000 | 0.040 | 19 | 19944193 | intron variant | G/A;C | snv | 1 | |||
rs7250793 | 1.000 | 0.040 | 19 | 19925055 | intron variant | T/C | snv | 0.88 | 1 | ||
rs11563346 | 1.000 | 0.040 | 7 | 127368435 | intron variant | A/G | snv | 0.13 | 1 | ||
rs11563463 | 1.000 | 0.040 | 7 | 127366874 | intron variant | C/T | snv | 0.32 | 1 | ||
rs11563634 | 1.000 | 0.040 | 7 | 127367715 | intron variant | C/G | snv | 0.15 | 1 | ||
rs2285337 | 1.000 | 0.040 | 7 | 127367931 | intron variant | G/A | snv | 0.16 | 1 | ||
rs2285338 | 1.000 | 0.040 | 7 | 127368376 | intron variant | C/A;G | snv | 0.64 | 1 | ||
rs17815373 | 1.000 | 0.040 | 19 | 56097531 | intron variant | G/A | snv | 0.15 | 1 | ||
rs562907 | 1.000 | 0.040 | 19 | 56100455 | intron variant | G/A;T | snv | 1 | |||
rs685117 | 1.000 | 0.040 | 19 | 56111849 | intron variant | G/A;C | snv | 0.85 | 1 | ||
rs8103672 | 1.000 | 0.040 | 19 | 56119948 | intron variant | G/A;C | snv | 1 | |||
rs11672966 | 1.000 | 0.040 | 19 | 23095699 | intron variant | G/A | snv | 6.1E-02 | 1 | ||
rs1473419 | 1.000 | 0.040 | 19 | 23101548 | intron variant | C/T | snv | 0.54 | 1 | ||
rs1693286 | 1.000 | 0.040 | 19 | 23096201 | intron variant | C/A;G;T | snv | 0.15 | 1 | ||
rs1693294 | 1.000 | 0.040 | 19 | 23094893 | intron variant | C/A;T | snv | 1 | |||
rs2035172 | 1.000 | 0.040 | 19 | 23121702 | intron variant | T/C | snv | 0.12 | 1 |