Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1379188099
rs1379188099
CSHL1 ; GH1 ; LOC112268204
0.010 GeneticVariation BEFREE Since the GH deficiency was not total, additional binding and signaling studies were performed, which revealed that the GH-P59L variant displays some of the common features of bioinactive GH syndrome. 21546299

2011