| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28362459 | 0.925 | 0.040 | 19 | 5844781 | missense variant | A/C;G;T | snv | 0.18; 1.2E-05 | 3 | ||
| rs2923008 | 1.000 | 0.040 | 6 | 31349134 | intron variant | G/A;T | snv | 3 | |||
| rs3132374 | 1.000 | 0.040 | 6 | 28900717 | downstream gene variant | C/G | snv | 5.3E-02 | 3 | ||
| rs34459162 | 1.000 | 0.040 | 19 | 49542659 | missense variant | T/A;C | snv | 4.4E-05; 7.8E-02 | 3 | ||
| rs3848403 | 1.000 | 0.040 | 17 | 82736023 | intron variant | C/T | snv | 0.49 | 3 | ||
| rs413988 | 1.000 | 0.040 | 5 | 698535 | intergenic variant | C/G;T | snv | 3 | |||
| rs4253778 | 1.000 | 0.040 | 22 | 46234737 | intron variant | G/C;T | snv | 3 | |||
| rs5418 | 1.000 | 0.040 | 17 | 7281773 | 5 prime UTR variant | G/A | snv | 0.49 | 3 | ||
| rs56013828 | 1.000 | 0.040 | 6 | 131511584 | intron variant | G/A | snv | 0.20 | 3 | ||
| rs60307791 | 1.000 | 0.040 | 11 | 65767714 | intron variant | TT/-;T;TTT;TTTT | delins | 3 | |||
| rs6145546 | 1.000 | 0.040 | 15 | 45376406 | intron variant | CTCTTCAGGAAG/-;CTCTTCAGGAAGCTCTTCAGGAAG | delins | 3 | |||
| rs61742093 | 1.000 | 0.040 | 6 | 27912204 | missense variant | A/G | snv | 4.8E-02 | 5.5E-02 | 3 | |
| rs6978712 | 1.000 | 0.040 | 7 | 127507709 | intergenic variant | C/T | snv | 0.11 | 3 | ||
| rs70961709 | 1.000 | 0.040 | 3 | 186620652 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 | 3 | ||
| rs74375025 | 1.000 | 0.040 | 10 | 16905665 | intron variant | G/A | snv | 8.1E-02 | 3 | ||
| rs7539020 | 1.000 | 0.040 | 1 | 230713444 | intron variant | C/T | snv | 0.43 | 3 | ||
| rs7690819 | 1.000 | 0.040 | 4 | 111199502 | intergenic variant | A/G;T | snv | 3 | |||
| rs77559408 | 1.000 | 0.040 | 2 | 137542339 | intron variant | T/C | snv | 3.2E-02 | 3 | ||
| rs8026743 | 1.000 | 0.040 | 15 | 38937539 | intron variant | G/A | snv | 0.29 | 3 | ||
| rs867232360 | 1.000 | 0.040 | 7 | 44145552 | missense variant | C/T | snv | 3 | |||
| rs920435389 | 1.000 | 0.040 | 5 | 177091064 | missense variant | G/C | snv | 3 | |||
| rs1013773109 | 1.000 | 0.040 | 2 | 164497436 | missense variant | T/C | snv | 2.1E-05 | 2 | ||
| rs1036915 | 1.000 | 0.040 | 9 | 84822934 | intron variant | A/G | snv | 0.40 | 2 | ||
| rs1042488900 | 1.000 | 0.040 | 1 | 161802188 | synonymous variant | C/T | snv | 2 | |||
| rs1042615 | 1.000 | 0.040 | 12 | 63150429 | missense variant | A/C;G;T | snv | 0.60; 1.2E-05 | 2 |