Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1064156 | 1.000 | 0.080 | 9 | 130878519 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
rs121913456 | 1.000 | 0.080 | 9 | 130862943 | missense variant | A/G | snv | 1 | |||
rs121913457 | 1.000 | 0.080 | 9 | 130873004 | missense variant | T/C | snv | 1 | |||
rs34549764 | 1.000 | 0.080 | 9 | 130862953 | missense variant | A/G | snv | 2.6E-03 | 2.5E-03 | 1 | |
rs886063722 | 1.000 | 0.080 | 9 | 136677118 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
rs6931104 | 1.000 | 0.080 | 6 | 151465042 | intron variant | G/A | snv | 0.54 | 1 | ||
rs532354124 | 1.000 | 0.080 | 1 | 197103274 | missense variant | T/C;G | snv | 1 | |||
rs755796482 | 1.000 | 0.080 | 12 | 111447512 | missense variant | G/A | snv | 4.1E-06 | 8.1E-06 | 1 | |
rs766124888 | 1.000 | 0.080 | 22 | 23253817 | missense variant | C/A;G | snv | 4.0E-06; 4.0E-06 | 1 | ||
rs768288452 | 1.000 | 0.080 | 22 | 23181822 | missense variant | A/G | snv | 4.1E-06 | 1 | ||
rs1487152821 | 1.000 | 0.080 | 6 | 33180274 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
rs375912312 | 1.000 | 0.080 | 1 | 22588916 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
rs754541813 | 1.000 | 0.080 | 3 | 58123401 | synonymous variant | C/T | snv | 6.8E-05 | 2.8E-05 | 1 | |
rs1343187782 | 1.000 | 0.080 | 3 | 37298923 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
rs281860566 | 1.000 | 0.080 | 6 | 31270339 | missense variant | C/T | snv | 1 | |||
rs760454379 | 1.000 | 0.080 | 7 | 50400082 | missense variant | G/A | snv | 1.6E-05 | 7.0E-06 | 1 | |
rs12573787 | 1.000 | 0.080 | 10 | 87863959 | 5 prime UTR variant | G/A;C | snv | 1 | |||
rs1257378 | 1.000 | 0.080 | 11 | 94621792 | intron variant | A/T | snv | 1 | |||
rs137852974 | 0.925 | 0.200 | 11 | 62691132 | stop gained | G/A | snv | 4.0E-06 | 1 | ||
rs9610915 | 1.000 | 0.080 | 22 | 38215073 | 3 prime UTR variant | C/G | snv | 0.48 | 0.41 | 1 | |
rs754736070 | 1.000 | 0.080 | 4 | 99597206 | missense variant | T/C | snv | 8.0E-06 | 7.0E-06 | 1 | |
rs1414109649 | 1.000 | 0.080 | 5 | 40765164 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
rs369488601 | 1.000 | 0.080 | 22 | 23181175 | missense variant | G/A;C | snv | 1.9E-05; 9.7E-05 | 1 | ||
rs775014154 | 1.000 | 0.080 | 22 | 23181637 | missense variant | C/T | snv | 5.8E-05 | 7.0E-05 | 1 | |
rs267607040 | 0.851 | 0.320 | 18 | 44951948 | missense variant | G/A | snv | 1 |