| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2251746 | 0.882 | 0.120 | 1 | 159302270 | intron variant | T/C | snv | 0.20 | 3 | ||
| rs3001978 | 0.882 | 0.160 | 1 | 152153991 | 3 prime UTR variant | T/C | snv | 0.50 | 3 | ||
| rs7518129 | 0.882 | 0.120 | 1 | 173194429 | intron variant | A/G | snv | 0.47 | 3 | ||
| rs7534334 | 0.882 | 0.160 | 1 | 153205376 | downstream gene variant | C/T | snv | 0.25 | 3 | ||
| rs761212672 | 0.882 | 0.120 | 1 | 152304999 | stop gained | G/T | snv | 3.2E-05 | 3 | ||
| rs10910095 | 1.000 | 0.040 | 1 | 2579316 | upstream gene variant | G/A;C | snv | 2 | |||
| rs11204971 | 0.925 | 0.120 | 1 | 152286602 | intron variant | A/G | snv | 0.15 | 2 | ||
| rs113136594 | 0.925 | 0.120 | 1 | 152313436 | missense variant | G/A;C;T | snv | 6.0E-04; 4.0E-06; 8.0E-06 | 2 | ||
| rs12568784 | 0.925 | 0.120 | 1 | 152350656 | stop gained | G/A;T | snv | 0.24 | 0.21 | 2 | |
| rs1443712053 | 0.925 | 0.120 | 1 | 152310672 | stop gained | G/C | snv | 4.0E-06 | 2 | ||
| rs145627745 | 0.925 | 0.120 | 1 | 152313145 | missense variant | T/A | snv | 7.8E-03 | 8.0E-03 | 2 | |
| rs16833974 | 0.925 | 0.120 | 1 | 152354040 | missense variant | T/C | snv | 1.6E-02 | 6.1E-02 | 2 | |
| rs180768115 | 0.925 | 0.120 | 1 | 152310342 | stop gained | G/C;T | snv | 8.0E-06; 1.7E-04 | 2 | ||
| rs2066446 | 0.925 | 0.120 | 1 | 67315434 | intron variant | A/G | snv | 0.20 | 2 | ||
| rs28441202 | 0.925 | 0.120 | 1 | 152156387 | missense variant | A/G | snv | 2 | |||
| rs3856261 | 1.000 | 0.040 | 1 | 155906822 | intron variant | G/A | snv | 0.36 | 2 | ||
| rs560912365 | 0.925 | 0.120 | 1 | 152309046 | stop gained | C/G;T | snv | 4.0E-06; 2.2E-04 | 2 | ||
| rs6693927 | 0.925 | 0.120 | 1 | 153071533 | upstream gene variant | G/A | snv | 0.35 | 2 | ||
| rs748135905 | 0.925 | 0.120 | 1 | 152309045 | stop gained | C/A;T | snv | 4.0E-06; 2.8E-05 | 2 | ||
| rs76167968 | 1.000 | 0.040 | 1 | 35216137 | intergenic variant | T/C | snv | 0.25 | 2 | ||
| rs877776 | 0.925 | 0.120 | 1 | 152205542 | intron variant | C/G;T | snv | 2 | |||
| rs10489854 | 1.000 | 0.040 | 1 | 159279069 | non coding transcript exon variant | C/T | snv | 8.3E-02 | 1 | ||
| rs11265449 | 1.000 | 0.040 | 1 | 160612458 | intron variant | C/G | snv | 0.45 | 0.36 | 1 | |
| rs11466681 | 1.000 | 0.040 | 1 | 1206007 | intron variant | C/T | snv | 6.1E-02 | 1 | ||
| rs114997373 | 1.000 | 0.040 | 1 | 45535906 | downstream gene variant | G/A | snv | 1.2E-02 | 1 |