rs200801099, AR

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Reifenstein Syndrome
CUI: C0268301
Disease: Reifenstein Syndrome
0.010 GeneticVariation BEFREE A novel mutation F826L in the human androgen receptor in partial androgen insensitivity syndrome; increased NH2-/COOH-terminal domain interaction and TIF2 co-activation. 18656523 2008