| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3751667 | 1.000 | 0.040 | 16 | 954554 | synonymous variant | C/T | snv | 0.28 | 0.29 | 4 | |
| rs3791675 | 1.000 | 0.040 | 2 | 55884174 | intron variant | C/T | snv | 0.20 | 4 | ||
| rs3851634 | 0.882 | 0.040 | 12 | 106419124 | intron variant | T/C | snv | 0.22 | 4 | ||
| rs59060240 | 0.882 | 0.040 | 7 | 55080369 | intron variant | AA/-;A;AAA;AAAA;AAAAAAAAAAA | delins | 4 | |||
| rs6062302 | 0.882 | 0.040 | 20 | 63689615 | synonymous variant | T/C | snv | 0.74 | 0.81 | 4 | |
| rs648044 | 0.882 | 0.040 | 11 | 114160077 | non coding transcript exon variant | A/G;T | snv | 4 | |||
| rs723527 | 0.882 | 0.040 | 7 | 55067179 | intron variant | A/G | snv | 0.53 | 4 | ||
| rs75061358 | 0.882 | 0.040 | 7 | 54848587 | intergenic variant | T/C;G | snv | 4 | |||
| rs10131 | 1.000 | 0.040 | 13 | 108207498 | 3 prime UTR variant | C/T | snv | 0.12 | 3 | ||
| rs10464870 | 0.882 | 0.040 | 8 | 129465577 | intron variant | C/T | snv | 0.80 | 3 | ||
| rs1052555 | 0.882 | 0.040 | 19 | 45352266 | synonymous variant | G/A | snv | 0.28 | 0.26 | 3 | |
| rs117677079 | 0.882 | 0.040 | 4 | 121673909 | intron variant | T/C | snv | 8.3E-03 | 3 | ||
| rs13332653 | 0.882 | 0.040 | 16 | 24578078 | intergenic variant | T/G | snv | 0.11 | 3 | ||
| rs1346787 | 0.882 | 0.040 | 2 | 55865477 | downstream gene variant | C/A;G;T | snv | 3 | |||
| rs145929329 | 0.882 | 0.040 | 9 | 22066213 | intron variant | TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTTTTT | delins | 0.58 | 3 | ||
| rs2033214 | 0.882 | 0.040 | 16 | 24566199 | intron variant | T/G | snv | 0.14 | 3 | ||
| rs6470745 | 0.882 | 0.040 | 8 | 129629675 | intron variant | A/G | snv | 0.18 | 3 | ||
| rs7115578 | 0.882 | 0.040 | 11 | 96266936 | intron variant | G/A | snv | 0.37 | 3 | ||
| rs7502563 | 0.882 | 0.040 | 17 | 80947993 | intron variant | G/A | snv | 0.34 | 3 | ||
| rs9933544 | 0.882 | 0.040 | 16 | 24576962 | downstream gene variant | A/C | snv | 0.29 | 3 | ||
| rs10131032 | 1.000 | 0.040 | 14 | 32780875 | intron variant | G/A | snv | 9.3E-02 | 2 | ||
| rs10494090 | 1.000 | 0.040 | 1 | 108150714 | intron variant | A/C;G;T | snv | 2 | |||
| rs1058319 | 1.000 | 0.040 | 20 | 63743036 | 3 prime UTR variant | C/A;T | snv | 0.21 | 2 | ||
| rs1064794096 | 1.000 | 0.040 | 10 | 87864514 | missense variant | A/C;T | snv | 2 | |||
| rs10924303 | 1.000 | 0.040 | 1 | 245683732 | intron variant | C/T | snv | 0.15 | 2 |