rs61884288(G;G)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs61884288 |
| Gene | SAA1, HPS5 |
| Chromosome | 11 |
| Position | 18,281,986 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 1 | Likely to be benign; but was previously considered to be associated with Hermansky-Pudlak syndrome, type 5 |
| (A;G) | 1 | Likely benign, actually; but formerly considered a carrier of a reported Hermansky-Pudlak mutation |
| (G;G) | 0 | common in clinvar |
