Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1290141855 | 1.000 | 0.040 | 16 | 55698539 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 3 | |
rs10055255 | 1.000 | 0.040 | 5 | 76968168 | intron variant | A/T | snv | 0.50 | 2 | ||
rs10914456 | 1.000 | 0.040 | 1 | 31622570 | intron variant | T/C | snv | 0.51 | 2 | ||
rs10997870 | 1.000 | 0.040 | 10 | 67908257 | intron variant | G/T | snv | 0.47 | 2 | ||
rs161645 | 1.000 | 0.040 | 5 | 104734216 | intron variant | A/G | snv | 0.77 | 2 | ||
rs228644 | 1.000 | 0.080 | 1 | 7806023 | intron variant | G/A | snv | 0.36 | 2 | ||
rs3821831 | 1.000 | 0.040 | 3 | 52819385 | splice region variant | C/T | snv | 0.29 | 0.29 | 2 | |
rs7208505 | 1.000 | 0.040 | 17 | 59110368 | 3 prime UTR variant | G/A;C;T | snv | 2 | |||
rs736408 | 1.000 | 0.040 | 3 | 52801338 | intron variant | C/T | snv | 0.47 | 2 | ||
rs17466684 | 0.925 | 0.120 | 8 | 27595330 | downstream gene variant | G/A | snv | 0.15 | 5 | ||
rs112025902 | 0.925 | 0.080 | 4 | 120232669 | intron variant | A/G;T | snv | 4 | |||
rs115482041 | 0.925 | 0.080 | 9 | 4860267 | missense variant | C/T | snv | 2.6E-03 | 2.3E-03 | 4 | |
rs1876831 | 0.925 | 0.040 | 17 | 45830379 | non coding transcript exon variant | C/G;T | snv | 4.4E-06; 0.14 | 4 | ||
rs6191 | 0.925 | 0.040 | 5 | 143278591 | 3 prime UTR variant | C/A | snv | 0.48 | 4 | ||
rs1207568 | 0.925 | 0.120 | 13 | 33016046 | upstream gene variant | G/A | snv | 0.17 | 3 | ||
rs12720208 | 0.925 | 0.040 | 8 | 16992890 | 3 prime UTR variant | G/A | snv | 5.5E-02 | 3 | ||
rs2228305 | 0.925 | 0.120 | 17 | 82084916 | missense variant | C/T | snv | 4.1E-02 | 4.5E-02 | 3 | |
rs80356773 | 0.925 | 0.080 | 1 | 155235002 | missense variant | C/T | snv | 3 | |||
rs936306 | 0.925 | 0.080 | 15 | 51287401 | intron variant | C/T | snv | 0.30 | 3 | ||
rs9536314 | 0.925 | 0.160 | 13 | 33054001 | missense variant | T/A;G | snv | 0.14 | 3 | ||
rs1409851868 | 0.882 | 0.080 | 3 | 89399325 | missense variant | A/G | snv | 6 | |||
rs2239547 | 0.882 | 0.040 | 3 | 52821213 | intron variant | T/C | snv | 0.27 | 6 | ||
rs1220000453 | 0.882 | 0.120 | 11 | 58624189 | synonymous variant | C/T | snv | 5 | |||
rs680244 | 0.882 | 0.120 | 15 | 78578946 | intron variant | T/C | snv | 0.60 | 4 | ||
rs757891309 | 0.882 | 0.120 | 1 | 236850389 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 4 |