Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2075559 | 0.882 | 0.040 | 17 | 50189930 | intron variant | G/A;C;T | snv | 0.52; 4.0E-06 | 3 | ||
rs2236947 | 0.882 | 0.040 | 3 | 50334001 | intron variant | C/A | snv | 0.39 | 3 | ||
rs231755 | 0.882 | 0.040 | 2 | 203888846 | regulatory region variant | G/C | snv | 0.11 | 3 | ||
rs235764 | 0.882 | 0.040 | 20 | 6773599 | intron variant | G/A | snv | 0.31 | 3 | ||
rs29001322 | 0.882 | 0.040 | 10 | 97462918 | non coding transcript exon variant | A/C;G | snv | 3 | |||
rs3787547 | 0.882 | 0.040 | 20 | 54067899 | intron variant | G/A | snv | 0.36 | 3 | ||
rs4148416 | 0.882 | 0.040 | 17 | 50676062 | synonymous variant | C/T | snv | 8.7E-02 | 0.10 | 3 | |
rs454006 | 0.882 | 0.040 | 19 | 53886867 | intron variant | T/C | snv | 0.36 | 3 | ||
rs58834075 | 0.882 | 0.040 | 14 | 101066756 | non coding transcript exon variant | C/G;T | snv | 4.0E-06; 4.6E-02 | 3 | ||
rs756673959 | 0.882 | 0.040 | 12 | 68828867 | stop lost | T/G | snv | 3 | |||
rs758300152 | 0.882 | 0.040 | 14 | 44504889 | missense variant | T/C;G | snv | 1.6E-05; 4.0E-06 | 3 | ||
rs7591996 | 0.882 | 0.040 | 2 | 6321289 | intron variant | A/C | snv | 0.57 | 3 | ||
rs763098116 | 0.925 | 0.040 | 17 | 7673790 | missense variant | C/A;T | snv | 4.0E-06 | 3 | ||
rs764191858 | 0.882 | 0.040 | 4 | 185502359 | missense variant | G/A | snv | 3 | |||
rs770771727 | 0.882 | 0.040 | 6 | 144751941 | missense variant | A/C;G | snv | 4.5E-05; 2.5E-05 | 3 | ||
rs779591039 | 0.882 | 0.040 | 20 | 45253712 | missense variant | G/A | snv | 3 | |||
rs780673045 | 0.882 | 0.040 | 12 | 68839592 | missense variant | A/G | snv | 1.2E-05 | 3 | ||
rs8103992 | 0.882 | 0.040 | 19 | 19554834 | regulatory region variant | A/C;T | snv | 3 | |||
rs9866361 | 0.882 | 0.040 | 3 | 179190061 | intron variant | G/A | snv | 0.24 | 3 | ||
rs998074 | 0.882 | 0.040 | 6 | 160047351 | intron variant | T/A;C | snv | 0.53 | 3 | ||
rs998075 | 0.882 | 0.040 | 6 | 160047246 | synonymous variant | A/G | snv | 0.53 | 0.54 | 3 | |
rs1332788424 | 1.000 | 0.040 | 6 | 33009477 | synonymous variant | C/A;T | snv | 4.3E-06 | 2 | ||
rs12146774 | 1.000 | 0.040 | 12 | 119235698 | intron variant | C/T | snv | 0.15 | 1 | ||
rs137853008 | 1.000 | 0.040 | 22 | 28734673 | missense variant | C/A | snv | 1 | |||
rs2086452 | 1.000 | 0.040 | 15 | 100188458 | intron variant | G/A;C | snv | 1 |