| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12076373 | 1.000 | 0.040 | 1 | 243688645 | intron variant | G/C | snv | 0.20 | 2 | ||
| rs12088062 | 1.000 | 0.040 | 1 | 244811284 | intergenic variant | C/T | snv | 0.20 | 2 | ||
| rs12125049 | 1.000 | 0.040 | 1 | 60202030 | intergenic variant | C/T | snv | 0.12 | 2 | ||
| rs12723208 | 1.000 | 0.040 | 1 | 211337552 | intron variant | A/G | snv | 0.13 | 2 | ||
| rs1409785 | 1.000 | 0.040 | 1 | 74782438 | intergenic variant | G/A | snv | 0.65 | 2 | ||
| rs16838813 | 1.000 | 0.040 | 1 | 4364085 | intergenic variant | G/A;T | snv | 0.11 | 2 | ||
| rs17110757 | 1.000 | 0.040 | 1 | 54584133 | intron variant | G/A | snv | 0.20 | 2 | ||
| rs2427824 | 1.000 | 0.040 | 1 | 159295272 | intron variant | T/C | snv | 0.79 | 2 | ||
| rs2494262 | 1.000 | 0.040 | 1 | 159283882 | upstream gene variant | C/A;G | snv | 2 | |||
| rs4252707 | 1.000 | 0.040 | 1 | 204539019 | intron variant | G/A | snv | 0.17 | 2 | ||
| rs4845964 | 1.000 | 0.040 | 1 | 10920487 | regulatory region variant | G/A | snv | 0.36 | 2 | ||
| rs1048771 | 1.000 | 0.040 | 1 | 46278228 | synonymous variant | C/A;T | snv | 4.0E-06; 0.15 | 1 | ||
| rs781754593 | 1.000 | 0.040 | 1 | 12202039 | missense variant | A/G | snv | 4.2E-06 | 1 | ||
| rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 | ||
| rs121913500 | 0.529 | 0.600 | 2 | 208248388 | missense variant | C/A;G;T | snv | 4.0E-06 | 96 | ||
| rs121913499 | 0.605 | 0.520 | 2 | 208248389 | missense variant | G/A;C;T | snv | 51 | |||
| rs1045485 | 0.637 | 0.480 | 2 | 201284866 | missense variant | G/A;C;T | snv | 4.0E-06; 9.0E-02 | 34 | ||
| rs895520 | 0.689 | 0.320 | 2 | 100961475 | intron variant | G/A | snv | 0.35 | 23 | ||
| rs10165970 | 0.708 | 0.320 | 2 | 100840527 | intron variant | G/A | snv | 0.16 | 18 | ||
| rs17024869 | 0.708 | 0.320 | 2 | 100843581 | intron variant | T/C | snv | 8.3E-02 | 18 | ||
| rs7581886 | 0.708 | 0.320 | 2 | 100964784 | intron variant | C/T | snv | 0.92 | 18 | ||
| rs371074389 | 0.732 | 0.320 | 2 | 136115226 | synonymous variant | C/T | snv | 4.0E-06 | 4.2E-05 | 16 | |
| rs766914563 | 0.732 | 0.320 | 2 | 136115082 | synonymous variant | C/T | snv | 7.0E-06 | 16 | ||
| rs781172058 | 0.732 | 0.320 | 2 | 136115340 | synonymous variant | C/T | snv | 4.0E-06 | 16 | ||
| rs11554137 | 0.742 | 0.040 | 2 | 208248468 | synonymous variant | G/A | snv | 5.1E-02 | 6.8E-02 | 13 |