| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10900213 | 1.000 | 0.080 | 10 | 45409266 | intron variant | G/A;T | snv | 1 | |||
| rs2228064 | 1.000 | 0.080 | 10 | 45382602 | synonymous variant | G/A;C | snv | 3.6E-02 | 1 | ||
| rs17222814 | 1.000 | 0.080 | 13 | 30725416 | intron variant | G/A | snv | 6.9E-02 | 1 | ||
| rs4293222 | 1.000 | 0.080 | 13 | 30737636 | intron variant | C/A;G | snv | 1 | |||
| rs9315050 | 1.000 | 0.080 | 13 | 30761908 | intron variant | A/G | snv | 0.11 | 1 | ||
| rs11542029 | 1.000 | 0.080 | 19 | 44907864 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06; 1.2E-05 | 1 | ||
| rs4480162 | 1.000 | 0.080 | 8 | 1906649 | intron variant | G/C | snv | 0.25 | 1 | ||
| rs10431036 | 1.000 | 0.080 | 11 | 112176338 | 5 prime UTR variant | G/A | snv | 0.11 | 1 | ||
| rs7082237 | 1.000 | 0.080 | 10 | 130091533 | intron variant | C/A;T | snv | 1 | |||
| rs3745565 | 1.000 | 0.080 | 19 | 6690971 | intron variant | C/G | snv | 0.11 | 1 | ||
| rs1017119 | 1.000 | 0.080 | 9 | 121045260 | intron variant | T/C | snv | 2.0E-02 | 1 | ||
| rs3179089 | 1.000 | 0.080 | 14 | 90407068 | 3 prime UTR variant | C/G | snv | 0.39 | 1 | ||
| rs2686342 | 1.000 | 0.080 | 12 | 121247385 | intron variant | T/A;C | snv | 1 | |||
| rs190323149 | 1.000 | 0.080 | 5 | 149430704 | mature miRNA variant | C/T | snv | 4.1E-06 | 1 | ||
| rs752118 | 1.000 | 0.080 | 20 | 46118099 | upstream gene variant | C/T | snv | 0.19 | 1 | ||
| rs11572061 | 1.000 | 0.080 | 6 | 44448340 | 3 prime UTR variant | A/G | snv | 8.7E-03 | 1 | ||
| rs3176471 | 1.000 | 0.080 | 1 | 50973784 | intron variant | A/T | snv | 1.5E-02 | 1 | ||
| rs4771674 | 1.000 | 0.080 | 13 | 110386723 | intron variant | A/G | snv | 0.53 | 1 | ||
| rs3117604 | 1.000 | 0.080 | 4 | 73868951 | upstream gene variant | T/C | snv | 0.47 | 1 | ||
| rs12459936 | 1.000 | 0.080 | 19 | 15882231 | intron variant | C/G;T | snv | 1 | |||
| rs3093144 | 1.000 | 0.080 | 19 | 15891487 | intron variant | C/T | snv | 0.18 | 1 | ||
| rs3093193 | 1.000 | 0.080 | 19 | 15881104 | intron variant | C/G;T | snv | 1 | |||
| rs17579352 | 1.000 | 0.080 | 1 | 57885133 | intron variant | C/T | snv | 2.6E-02 | 1 | ||
| rs758203894 | 1.000 | 0.080 | 6 | 151842600 | synonymous variant | A/G | snv | 7.0E-06 | 1 | ||
| rs138364069 | 1.000 | 0.080 | 1 | 50832533 | intron variant | C/T | snv | 1.5E-02 | 1 |