rs104894182(A;G)
From SNPedia
| Carrier of a hemophagocytic lymphohistiocytosis (HLH) mutation |
| Is a | genotype |
| of | rs104894182 |
| Gene | PRF1 |
| Chromosome | 10 |
| Position | 70,598,885 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 3 | Carrier of a hemophagocytic lymphohistiocytosis (HLH) mutation |
| (G;G) | 0 | common in clinvar |
Unaffected in absence of a second PRF1 gene mutation; see links via main rs-page.
