Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs5443 | 0.532 | 0.760 | 12 | 6845711 | synonymous variant | C/T | snv | 0.36 | 0.44 | 106 | |
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 98 | ||
rs1137101 | 0.554 | 0.760 | 1 | 65592830 | missense variant | A/G | snv | 0.51 | 0.50 | 77 | |
rs17782313 | 0.683 | 0.480 | 18 | 60183864 | intergenic variant | T/C | snv | 0.24 | 34 | ||
rs572169 | 0.882 | 0.160 | 3 | 172447937 | synonymous variant | C/T | snv | 0.31 | 0.24 | 6 | |
rs5574 | 0.882 | 0.200 | 7 | 24289514 | synonymous variant | C/T | snv | 0.43 | 0.43 | 5 | |
rs1051168 | 1.000 | 0.080 | 15 | 84657289 | missense variant | G/C;T | snv | 4.5E-06; 0.22 | 2 | ||
rs1258628899 | 17 | 43953174 | synonymous variant | G/A | snv | 7.0E-06 | 1 | ||||
rs2878329 | 19 | 9215066 | intron variant | C/T | snv | 0.14 | 1 | ||||
rs781443388 | 4 | 155214416 | synonymous variant | G/A | snv | 1.6E-05 | 2.1E-05 | 1 | |||
rs992472 | 20 | 32797463 | intron variant | G/T | snv | 0.49 | 1 | ||||
rs992990 | 10 | 26278252 | intron variant | C/A;G | snv | 0.37 | 1 |