| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs201821879 | 0.882 | 0.040 | 12 | 68809237 | missense variant | C/T | snv | 1.6E-04 | 1.9E-04 | 3 | |
| rs756673959 | 0.882 | 0.040 | 12 | 68828867 | stop lost | T/G | snv | 3 | |||
| rs780673045 | 0.882 | 0.040 | 12 | 68839592 | missense variant | A/G | snv | 1.2E-05 | 3 | ||
| rs12879262 | 0.882 | 0.040 | 14 | 102539710 | non coding transcript exon variant | G/C | snv | 0.12 | 0.11 | 3 | |
| rs58834075 | 0.882 | 0.040 | 14 | 101066756 | non coding transcript exon variant | C/G;T | snv | 4.0E-06; 4.6E-02 | 3 | ||
| rs29001322 | 0.882 | 0.040 | 10 | 97462918 | non coding transcript exon variant | A/C;G | snv | 3 | |||
| rs764191858 | 0.882 | 0.040 | 4 | 185502359 | missense variant | G/A | snv | 3 | |||
| rs9866361 | 0.882 | 0.040 | 3 | 179190061 | intron variant | G/A | snv | 0.24 | 3 | ||
| rs454006 | 0.882 | 0.040 | 19 | 53886867 | intron variant | T/C | snv | 0.36 | 3 | ||
| rs2236947 | 0.882 | 0.040 | 3 | 50334001 | intron variant | C/A | snv | 0.39 | 3 | ||
| rs763098116 | 0.925 | 0.040 | 17 | 7673790 | missense variant | C/A;T | snv | 4.0E-06 | 3 | ||
| rs770771727 | 0.882 | 0.040 | 6 | 144751941 | missense variant | A/C;G | snv | 4.5E-05; 2.5E-05 | 3 | ||
| rs1295925 | 0.882 | 0.040 | 17 | 59832902 | intron variant | T/C | snv | 0.60 | 3 | ||
| rs1215600806 | 0.851 | 0.120 | 1 | 21564100 | missense variant | T/C | snv | 1.2E-05 | 4 | ||
| rs1416572796 | 0.851 | 0.120 | 1 | 21568170 | missense variant | G/T | snv | 4.0E-06 | 4 | ||
| rs143358506 | 0.851 | 0.120 | 1 | 21560674 | missense variant | T/C | snv | 8.0E-06 | 7.0E-06 | 4 | |
| rs11866002 | 0.851 | 0.120 | 16 | 58553833 | synonymous variant | C/T | snv | 0.35 | 0.39 | 4 | |
| rs10019009 | 0.851 | 0.080 | 4 | 87661983 | missense variant | A/G;T | snv | 4.0E-06; 0.29 | 4 | ||
| rs4150506 | 0.851 | 0.120 | 2 | 127262970 | intron variant | G/A | snv | 0.18 | 4 | ||
| rs1906953 | 0.882 | 0.040 | 6 | 34068669 | intron variant | C/T | snv | 0.25 | 4 | ||
| rs4730222 | 0.851 | 0.040 | 7 | 107169848 | 5 prime UTR variant | G/A;C;T | snv | 4 | |||
| rs16948627 | 0.882 | 0.040 | 17 | 50063432 | intron variant | C/A;T | snv | 4 | |||
| rs2230392 | 0.882 | 0.040 | 17 | 50078061 | missense variant | G/A | snv | 0.14 | 9.0E-02 | 4 | |
| rs2285524 | 0.882 | 0.040 | 17 | 50073989 | synonymous variant | T/C | snv | 0.21 | 0.24 | 4 | |
| rs59267781 | 0.851 | 0.120 | 1 | 156138657 | missense variant | C/G | snv | 4 |