Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1235162 | 0.827 | 0.280 | 6 | 29569447 | intron variant | A/G | snv | 6.0E-02 | 6 | ||
rs2284178 | 0.925 | 0.120 | 6 | 31464348 | non coding transcript exon variant | C/T | snv | 0.44 | 6 | ||
rs2844513 | 0.925 | 0.120 | 6 | 31420437 | intron variant | G/A | snv | 0.53 | 6 | ||
rs527476195 | 0.925 | 0.120 | 6 | 31133165 | intron variant | G/A | snv | 6 | |||
rs14158 | 0.851 | 0.160 | 19 | 11131368 | synonymous variant | G/A | snv | 0.24 | 0.22 | 5 | |
rs7756521 | 1.000 | 6 | 30880476 | intron variant | T/C | snv | 0.25 | 5 | |||
rs3117143 | 0.882 | 0.160 | 6 | 29063365 | intron variant | C/A | snv | 5.2E-02 | 4 | ||
rs3749971 | 0.925 | 0.160 | 6 | 29374998 | missense variant | G/A | snv | 5.5E-02 | 5.7E-02 | 4 | |
rs1233579 | 0.925 | 0.160 | 6 | 28744886 | intergenic variant | A/G | snv | 7.2E-02 | 3 | ||
rs13194504 | 0.925 | 0.120 | 6 | 28662914 | intergenic variant | G/A | snv | 5.1E-02 | 3 | ||
rs3131093 | 0.925 | 0.160 | 6 | 28869660 | intergenic variant | C/T | snv | 7.1E-02 | 3 | ||
rs11884476 | 2 | 205453869 | intron variant | C/G | snv | 0.11 | 1 | ||||
rs1369619997 | 2 | 8731746 | missense variant | G/C | snv | 4.0E-06 | 1 | ||||
rs374596032 | 2 | 8813255 | missense variant | A/C;G | snv | 4.0E-06; 8.0E-06 | 1 | ||||
rs4118325 | 1 | 107035210 | intergenic variant | G/A;T | snv | 1 | |||||
rs6467710 | 7 | 137519073 | intron variant | G/A;C | snv | 1 | |||||
rs919266 | 19 | 17403506 | intron variant | T/C;G | snv | 1 |