rs745452577(A;G)
From SNPedia
| Of uncertain significance relative to Schwartz Jampel syndrome according to ClinVar |
| Is a | genotype |
| of | rs745452577 |
| Gene | HSPG2 |
| Chromosome | 1 |
| Position | 21,865,798 |
| mentioned | by |
| Magnitude | 1 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 1 | Of uncertain significance relative to Schwartz Jampel syndrome according to ClinVar |
| (G;G) | 0 | common in clinvar |
