Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12573787 | 1.000 | 0.080 | 10 | 87863959 | 5 prime UTR variant | G/A;C | snv | 1 | |||
rs1343187782 | 1.000 | 0.080 | 3 | 37298923 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
rs1414109649 | 1.000 | 0.080 | 5 | 40765164 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
rs1487152821 | 1.000 | 0.080 | 6 | 33180274 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
rs281860566 | 1.000 | 0.080 | 6 | 31270339 | missense variant | C/T | snv | 1 | |||
rs34549764 | 1.000 | 0.080 | 9 | 130862953 | missense variant | A/G | snv | 2.6E-03 | 2.5E-03 | 1 | |
rs369488601 | 1.000 | 0.080 | 22 | 23181175 | missense variant | G/A;C | snv | 1.9E-05; 9.7E-05 | 1 | ||
rs375912312 | 1.000 | 0.080 | 1 | 22588916 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
rs4795519 | 1.000 | 0.080 | 17 | 27214252 | intergenic variant | A/C | snv | 0.43 | 1 | ||
rs532354124 | 1.000 | 0.080 | 1 | 197103274 | missense variant | T/C;G | snv | 1 | |||
rs6931104 | 1.000 | 0.080 | 6 | 151465042 | intron variant | G/A | snv | 0.54 | 1 | ||
rs754541813 | 1.000 | 0.080 | 3 | 58123401 | synonymous variant | C/T | snv | 6.8E-05 | 2.8E-05 | 1 | |
rs754736070 | 1.000 | 0.080 | 4 | 99597206 | missense variant | T/C | snv | 8.0E-06 | 7.0E-06 | 1 | |
rs755796482 | 1.000 | 0.080 | 12 | 111447512 | missense variant | G/A | snv | 4.1E-06 | 8.1E-06 | 1 | |
rs760454379 | 1.000 | 0.080 | 7 | 50400082 | missense variant | G/A | snv | 1.6E-05 | 7.0E-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 | ||
rs775014154 | 1.000 | 0.080 | 22 | 23181637 | missense variant | C/T | snv | 5.8E-05 | 7.0E-05 | 1 | |
rs886063722 | 1.000 | 0.080 | 9 | 136677118 | missense variant | 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 | |
rs121908587 | 0.827 | 0.120 | 4 | 54278380 | missense variant | C/T | snv | 6 | |||
rs387906517 | 0.827 | 0.120 | 9 | 130862919 | missense variant | G/A | snv | 6 | |||
rs121913448 | 0.827 | 0.120 | 9 | 130862976 | missense variant | G/A | snv | 5 | |||
rs121913461 | 0.851 | 0.120 | 9 | 130862970 | missense variant | T/C | snv | 5 | |||
rs1060500091 | 0.882 | 0.120 | 3 | 128481887 | missense variant | A/C | snv | 4 |