Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs200889048 | 0.882 | 0.120 | 3 | 74928276 | intergenic variant | C/- | del | 3 | |||
rs1800497 | 0.620 | 0.400 | 11 | 113400106 | missense variant | G/A | snv | 0.26 | 0.26 | 56 | |
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs746682028 | 0.645 | 0.480 | 11 | 27658414 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 36 | ||
rs554073050 | 0.925 | 0.040 | 3 | 42263460 | synonymous variant | G/A | snv | 1.2E-05 | 7.0E-06 | 3 | |
rs77600076 | 1.000 | 0.040 | 21 | 18159125 | intron variant | A/C | snv | 2.5E-02 | 1 | ||
rs1049353 | 0.630 | 0.600 | 6 | 88143916 | synonymous variant | C/T | snv | 0.21 | 0.20 | 42 | |
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs4818 | 0.683 | 0.440 | 22 | 19963684 | synonymous variant | C/G;T | snv | 0.34 | 27 | ||
rs4633 | 0.695 | 0.400 | 22 | 19962712 | synonymous variant | C/T | snv | 0.46 | 0.45 | 25 | |
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 98 | ||
rs696217 | 0.662 | 0.640 | 3 | 10289773 | missense variant | G/T | snv | 8.8E-02 | 7.1E-02 | 32 | |
rs495225 | 0.882 | 0.040 | 3 | 172448243 | synonymous variant | G/A;C;T | snv | 0.66 | 4 | ||
rs6296 | 0.732 | 0.160 | 6 | 77462543 | synonymous variant | C/G | snv | 0.31 | 0.27 | 23 | |
rs287103 | 1.000 | 0.040 | 19 | 33801816 | intron variant | A/G | snv | 0.67 | 1 | ||
rs12490016 | 0.882 | 0.120 | 3 | 157121142 | intron variant | G/C | snv | 4.6E-02 | 3 | ||
rs13338499 | 0.925 | 0.040 | 16 | 67486220 | intron variant | A/G;T | snv | 2 | |||
rs1445130 | 1.000 | 0.040 | 2 | 18653385 | regulatory region variant | A/G | snv | 0.12 | 1 | ||
rs52820871 | 0.827 | 0.160 | 18 | 60371599 | missense variant | T/G | snv | 6.9E-03 | 7.6E-03 | 6 | |
rs142014203 | 1.000 | 0.040 | 8 | 62346358 | intron variant | T/G | snv | 2.1E-02 | 1 | ||
rs53576 | 0.641 | 0.320 | 3 | 8762685 | intron variant | A/G;T | snv | 42 | |||
rs1042571 | 0.882 | 0.120 | 2 | 25161018 | 3 prime UTR variant | G/A | snv | 0.16 | 3 | ||
rs1630623 | 0.882 | 0.120 | 9 | 72725323 | intron variant | A/G | snv | 0.29 | 3 |