| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs748702477 | 1.000 | 0.080 | 10 | 77110278 | synonymous variant | A/G | snv | 1.4E-05 | 2 | ||
| rs10013040 | 1.000 | 0.080 | 4 | 177309998 | synonymous variant | C/A | snv | 0.20 | 0.20 | 1 | |
| rs1008563 | 1.000 | 0.080 | 2 | 218162165 | downstream gene variant | G/A | snv | 0.43 | 1 | ||
| rs10176176 | 1.000 | 0.080 | 2 | 85534925 | upstream gene variant | A/T | snv | 0.54 | 1 | ||
| rs10263017 | 1.000 | 0.080 | 7 | 6026173 | intron variant | G/C;T | snv | 1 | |||
| rs10281500 | 1.000 | 0.080 | 7 | 55475197 | intron variant | C/G | snv | 0.32 | 1 | ||
| rs1045274 | 1.000 | 0.080 | 16 | 580902 | synonymous variant | C/G;T | snv | 0.16; 2.0E-05 | 1 | ||
| rs104895285 | 1.000 | 0.080 | 12 | 6330873 | missense variant | A/T | snv | 1 | |||
| rs1049636 | 1.000 | 0.080 | 4 | 154604818 | 3 prime UTR variant | G/A | snv | 0.67 | 0.70 | 1 | |
| rs1050998 | 1.000 | 0.080 | 17 | 4735442 | missense variant | A/G | snv | 0.46 | 0.41 | 1 | |
| rs10518325 | 1.000 | 0.080 | 4 | 118796479 | intron variant | A/G | snv | 6.4E-02 | 1 | ||
| rs1058932 | 1.000 | 0.080 | 10 | 95037104 | 3 prime UTR variant | G/A | snv | 0.22 | 0.24 | 1 | |
| rs10788952 | 1.000 | 0.080 | 1 | 53272428 | non coding transcript exon variant | C/T | snv | 0.37 | 1 | ||
| rs10838532 | 1.000 | 0.080 | 11 | 45925913 | intron variant | G/C | snv | 0.18 | 1 | ||
| rs10889160 | 1.000 | 0.080 | 1 | 59896449 | intron variant | T/C | snv | 0.23 | 1 | ||
| rs1135402763 | 1.000 | 0.080 | 2 | 21032540 | missense variant | T/C;G | snv | 1 | |||
| rs1151640 | 1.000 | 0.080 | 1 | 247672648 | missense variant | T/C | snv | 0.46 | 0.36 | 1 | |
| rs11574915 | 1.000 | 0.080 | 9 | 34710087 | 5 prime UTR variant | A/C;G | snv | 0.13; 4.1E-06 | 1 | ||
| rs11666735 | 1.000 | 0.080 | 19 | 54885501 | missense variant | G/A | snv | 6.9E-02 | 6.6E-02 | 1 | |
| rs12027041 | 1.000 | 0.080 | 1 | 3674884 | intron variant | G/C | snv | 0.38 | 1 | ||
| rs12118721 | 1.000 | 0.080 | 1 | 154424940 | intron variant | T/C | snv | 0.51 | 1 | ||
| rs12316150 | 1.000 | 0.080 | 12 | 10159692 | 3 prime UTR variant | A/T | snv | 7.4E-02 | 1 | ||
| rs12363415 | 1.000 | 0.080 | 11 | 13377061 | intron variant | A/G | snv | 0.20 | 1 | ||
| rs12510359 | 1.000 | 0.080 | 4 | 168756241 | non coding transcript exon variant | A/G;T | snv | 0.50 | 1 | ||
| rs1275147925 | 1.000 | 0.080 | 19 | 44906613 | missense variant | A/G | snv | 7.0E-06 | 1 |