Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1014290 | 0.827 | 0.280 | 4 | 10000237 | intron variant | G/A | snv | 0.72 | 2 | ||
rs78154696 | 1.000 | 0.080 | 5 | 1000041 | upstream gene variant | G/A;T | snv | 1 | |||
rs9833888 | 1.000 | 0.080 | 3 | 100004736 | intron variant | G/T | snv | 0.18 | 1 | ||
rs10988944 | 0.925 | 0.040 | 9 | 100011933 | intron variant | C/A | snv | 0.20 | 2 | ||
rs7006527 | 0.851 | 0.040 | 8 | 100012277 | intron variant | A/C;T | snv | 3 | |||
rs7323466 | 13 | 100019615 | intergenic variant | T/C | snv | 0.64 | 1 | ||||
rs142529006 | 7 | 100022093 | intron variant | T/A | snv | 6.9E-03 | 4 | ||||
rs56079856 | 4 | 1000223 | intron variant | G/T | snv | 0.14 | 1 | ||||
rs7826222 | 1.000 | 0.080 | 8 | 10002570 | intron variant | G/C | snv | 1 | |||
rs1963304 | 7 | 100028173 | intron variant | T/A;G | snv | 1 | |||||
rs1015538 | 7 | 100028412 | intron variant | A/G | snv | 0.72 | 1 | ||||
rs2897075 | 1.000 | 0.040 | 7 | 100032719 | intron variant | C/T | snv | 0.31 | 1 | ||
rs10883437 | 1.000 | 0.040 | 10 | 100035604 | regulatory region variant | T/A;G | snv | 0.43 | 2 | ||
rs9585327 | 1.000 | 0.040 | 13 | 100037100 | intergenic variant | G/A | snv | 0.36 | 1 | ||
rs181978376 | 10 | 100037758 | downstream gene variant | T/A;C | snv | 1 | |||||
rs4486555 | 10 | 100039545 | downstream gene variant | G/T | snv | 0.40 | 1 | ||||
rs66803065 | 11 | 10004305 | intron variant | C/A;T | snv | 0.19 | 2 | ||||
rs4295981 | 10 | 100043668 | intron variant | C/T | snv | 0.37 | 1 | ||||
rs11599750 | 10 | 100045685 | intron variant | C/T | snv | 0.40 | 2 | ||||
rs4919420 | 10 | 100046495 | intron variant | A/G | snv | 0.40 | 1 | ||||
rs13001130 | 2 | 100052237 | intron variant | G/A | snv | 0.15 | 1 | ||||
rs397807524 | 15 | 100052239 | intron variant | -/AA | ins | 7.0E-06 | 1 | ||||
rs78633727 | 2 | 100052995 | intron variant | T/C | snv | 0.16 | 1 | ||||
rs6750720 | 2 | 100054283 | intron variant | C/G;T | snv | 1 | |||||
rs10209110 | 1.000 | 0.120 | 2 | 100056230 | intron variant | C/T | snv | 0.47 | 1 |