Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
rs1799971 | 0.559 | 0.600 | 6 | 154039662 | missense variant | A/G | snv | 0.19 | 0.12 | 95 | |
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 83 | ||
rs25531 | 0.581 | 0.520 | 17 | 30237328 | upstream gene variant | T/C | snv | 0.18 | 72 | ||
rs1800497 | 0.620 | 0.400 | 11 | 113400106 | missense variant | G/A | snv | 0.26 | 0.26 | 56 | |
rs324420 | 0.637 | 0.440 | 1 | 46405089 | missense variant | C/A | snv | 0.24 | 0.26 | 48 | |
rs6277 | 0.689 | 0.480 | 11 | 113412737 | synonymous variant | G/A | snv | 0.41 | 0.38 | 36 | |
rs1076560 | 0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 | 11 | ||
rs886205 | 0.827 | 0.360 | 12 | 111766623 | intron variant | A/G | snv | 0.35 | 8 | ||
rs4646437 | 0.827 | 0.200 | 7 | 99767460 | intron variant | G/A | snv | 0.30 | 8 | ||
rs279858 | 0.851 | 0.080 | 4 | 46312576 | synonymous variant | T/C | snv | 0.40 | 0.38 | 8 | |
rs13438494 | 1.000 | 0.040 | 7 | 82759398 | intron variant | T/G | snv | 0.61 | 6 | ||
rs1126671 | 0.851 | 0.120 | 4 | 99127263 | missense variant | T/C | snv | 0.76 | 0.75 | 5 | |
rs1042363 | 0.882 | 0.080 | 6 | 151356693 | 3 prime UTR variant | T/C | snv | 4 | |||
rs441 | 0.882 | 0.200 | 12 | 111791045 | intron variant | T/C | snv | 0.18 | 4 | ||
rs1800759 | 0.925 | 0.120 | 4 | 99144358 | intron variant | T/G | snv | 0.49 | 4 | ||
rs17228616 | 1.000 | 0.080 | 7 | 100890100 | 3 prime UTR variant | G/T | snv | 9.8E-02 | 3 | ||
rs17228602 | 7 | 100890786 | 3 prime UTR variant | C/T | snv | 1.5E-02 | 2 | ||||
rs4646440 | 7 | 99763247 | intron variant | G/A | snv | 5.1E-02 | 2 | ||||
rs1650420 | 1.000 | 0.080 | 16 | 10174473 | intron variant | T/C | snv | 0.58 | 2 | ||
rs199953844 | 6 | 154039650 | missense variant | C/A;T | snv | 4.0E-06; 1.2E-04 | 2 | ||||
rs10784339 | 12 | 63144866 | 3 prime UTR variant | G/A;C;T | snv | 1 | |||||
rs3743484 | 15 | 74752059 | intron variant | G/C | snv | 3.7E-02 | 1 |