Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057517041
rs1057517041
PROP1
A 0.700 GeneticVariation CLINVAR Human Prop-1: cloning, mapping, genomic structure. Mutations in familial combined pituitary hormone deficiency. 9824293

1998