Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs766673446
rs766673446
PROP1
A 0.700 GeneticVariation CLINVAR Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency. 26608600

2016
dbSNP: rs766673446
rs766673446
PROP1
A 0.700 GeneticVariation CLINVAR Recombinant human growth hormone replacement in a Japanese man with a novel PROP1 gene mutation (R112X). 22111336

2011