| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4795519 | 1.000 | 0.080 | 17 | 27214252 | intergenic variant | A/C | snv | 0.43 | 1 | ||
| rs1057519758 | 1.000 | 0.080 | 9 | 130872153 | missense variant | T/G | snv | 1 | |||
| rs1057519772 | 1.000 | 0.080 | 9 | 130872895 | missense variant | A/G | snv | 1 | |||
| rs1057519774 | 1.000 | 0.080 | 9 | 130872902 | missense variant | T/G | snv | 1 | |||
| rs1057519775 | 1.000 | 0.080 | 9 | 130873028 | missense variant | T/G | snv | 1 | |||
| rs1064156 | 1.000 | 0.080 | 9 | 130878519 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs121913449 | 1.000 | 0.080 | 9 | 130862977 | missense variant | A/T | snv | 1 | |||
| rs121913450 | 1.000 | 0.080 | 9 | 130873016 | missense variant | A/G | snv | 1 | |||
| rs121913453 | 1.000 | 0.080 | 9 | 130862962 | missense variant | G/A | snv | 1 | |||
| rs121913455 | 1.000 | 0.080 | 9 | 130862955 | missense variant | C/G | snv | 1 | |||
| rs121913456 | 1.000 | 0.080 | 9 | 130862943 | missense variant | A/G | snv | 1 | |||
| rs121913457 | 1.000 | 0.080 | 9 | 130873004 | missense variant | T/C | snv | 1 | |||
| rs121913458 | 1.000 | 0.080 | 9 | 130862969 | missense variant | G/C;T | snv | 1 | |||
| rs34549764 | 1.000 | 0.080 | 9 | 130862953 | missense variant | A/G | snv | 2.6E-03 | 2.5E-03 | 1 | |
| rs886063722 | 1.000 | 0.080 | 9 | 136677118 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs6931104 | 1.000 | 0.080 | 6 | 151465042 | intron variant | G/A | snv | 0.54 | 1 | ||
| rs532354124 | 1.000 | 0.080 | 1 | 197103274 | missense variant | T/C;G | snv | 1 | |||
| rs755796482 | 1.000 | 0.080 | 12 | 111447512 | missense variant | G/A | snv | 4.1E-06 | 8.1E-06 | 1 | |
| rs766124888 | 1.000 | 0.080 | 22 | 23253817 | missense variant | C/A;G | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs768288452 | 1.000 | 0.080 | 22 | 23181822 | missense variant | A/G | snv | 4.1E-06 | 1 | ||
| rs1487152821 | 1.000 | 0.080 | 6 | 33180274 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs1057519776 | 1.000 | 0.080 | 1 | 36467843 | missense variant | T/C | snv | 1 | |||
| rs375912312 | 1.000 | 0.080 | 1 | 22588916 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs754541813 | 1.000 | 0.080 | 3 | 58123401 | synonymous variant | C/T | snv | 6.8E-05 | 2.8E-05 | 1 | |
| rs1343187782 | 1.000 | 0.080 | 3 | 37298923 | missense variant | T/C | snv | 4.0E-06 | 1 |