Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11920090 | 1.000 | 0.040 | 3 | 170999732 | intron variant | T/A | snv | 0.20 | 3 | ||
rs3138708 | 3 | 171009914 | intron variant | T/G | snv | 3.1E-02 | 2 | ||||
rs5394 | 3 | 171027104 | intron variant | G/A | snv | 0.15 | 2 | ||||
rs4402960 | 0.724 | 0.400 | 3 | 185793899 | intron variant | G/T | snv | 0.38 | 4 | ||
rs7651090 | 0.925 | 0.080 | 3 | 185795604 | intron variant | A/G | snv | 0.39 | 3 | ||
rs7756992 | 0.827 | 0.240 | 6 | 20679478 | intron variant | A/G;T | snv | 4 | |||
rs9368222 | 1.000 | 0.080 | 6 | 20686765 | intron variant | C/A;T | snv | 5 | |||
rs17712208 | 1 | 213977102 | intron variant | T/A | snv | 2.1E-02 | 2 | ||||
rs340878 | 1 | 213983706 | intron variant | G/C | snv | 0.63 | 2 | ||||
rs340874 | 0.882 | 0.080 | 1 | 213985913 | non coding transcript exon variant | T/C | snv | 0.40 | 4 | ||
rs10811661 | 0.724 | 0.400 | 9 | 22134095 | intergenic variant | T/C | snv | 0.14 | 4 | ||
rs6113722 | 20 | 22576461 | intron variant | G/A;T | snv | 2 | |||||
rs1371614 | 2 | 26930006 | intron variant | C/T | snv | 0.29 | 3 | ||||
rs1124649 | 2 | 27037601 | missense variant | G/A | snv | 0.32 | 0.35 | 2 | |||
rs13404446 | 0.925 | 0.120 | 2 | 27296386 | intron variant | G/A | snv | 0.42 | 4 | ||
rs4665965 | 0.925 | 0.120 | 2 | 27313513 | intron variant | T/A;C | snv | 4 | |||
rs11891554 | 2 | 27390750 | intron variant | G/A;T | snv | 7.1E-02 | 2 | ||||
rs780110 | 0.925 | 0.120 | 2 | 27462521 | intron variant | G/A | snv | 0.56 | 4 | ||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 25 | |
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 24 | ||
rs2068834 | 0.925 | 0.120 | 2 | 27616672 | intron variant | T/C | snv | 0.28 | 10 | ||
rs13023194 | 0.925 | 0.120 | 2 | 27744393 | intergenic variant | G/A;C | snv | 4 | |||
rs2305929 | 1.000 | 0.040 | 2 | 27891044 | intron variant | A/G | snv | 0.14 | 3 | ||
rs11619319 | 13 | 27913462 | intron variant | A/G | snv | 0.23 | 2 | ||||
rs576674 | 1.000 | 0.080 | 13 | 32980164 | intergenic variant | G/A | snv | 0.69 | 2 |