Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11643024 | 16 | 11349326 | intron variant | A/G | snv | 0.67 | 2 | ||||
rs11549428 | 16 | 11254849 | missense variant | C/G;T | snv | 5.0E-03 | 1 | ||||
rs4781072 | 16 | 11366623 | intron variant | C/G;T | snv | 1 | |||||
rs35578928 | 16 | 11373920 | intron variant | G/A | snv | 0.15 | 1 | ||||
rs7188861 | 16 | 11360793 | intron variant | C/A | snv | 0.16 | 1 | ||||
rs367569 | 0.807 | 0.120 | 16 | 11271643 | intron variant | C/T | snv | 0.32 | 6 | ||
rs11074967 | 0.807 | 0.120 | 16 | 11377557 | intron variant | C/G | snv | 0.36 | 6 | ||
rs8061370 | 0.882 | 16 | 11364614 | intron variant | A/C;T | snv | 4 | ||||
rs4780355 | 0.882 | 0.120 | 16 | 11254001 | intron variant | T/C;G | snv | 2 | |||
rs12928822 | 0.882 | 0.200 | 16 | 11310036 | intron variant | C/T | snv | 0.13 | 1 | ||
rs423674 | 0.925 | 0.120 | 16 | 11279548 | intron variant | G/T | snv | 0.18 | 2 | ||
rs529866 | 1.000 | 0.040 | 16 | 11279463 | intron variant | C/T | snv | 0.18 | 2 | ||
rs1646019 | 1.000 | 0.080 | 16 | 11265823 | intron variant | C/T | snv | 0.36 | 1 | ||
rs80073729 | 1.000 | 0.080 | 16 | 11279940 | intron variant | G/A | snv | 4.1E-03 | 1 | ||
rs193778 | 1.000 | 0.120 | 16 | 11257354 | intron variant | A/G | snv | 0.20 | 1 | ||
rs77804393 | 1.000 | 0.040 | 16 | 11265296 | intron variant | G/A;T | snv | 1 | |||
rs77061563 | 1.000 | 0.040 | 16 | 11358685 | intron variant | C/G;T | snv | 1 | |||
rs7191700 | 1.000 | 0.080 | 16 | 11312946 | intron variant | C/T | snv | 0.27 | 1 | ||
rs6498184 | 1.000 | 0.080 | 16 | 11342133 | non coding transcript exon variant | T/A;C | snv | 1 |