{{Rsnum
|rsid=193922688
|Chromosome=5
|Orientation=minus
|geno1=(-;-)
|geno2=(-;AG)
|geno3=(AG;AG)
|Gene=PROP1
|position=177994146
|Gene_s=PROP1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922688
|Reversed=1
|FwdREF=AG
|FwdALT=
|REF=ACT
|ALT=A
|RSPOS=177421146
|CHROM=5
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100200
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.177421147_177421148delCT
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Pituitary hormone deficiency, combined 2; Pituitary hormone deficiency, combined
|Disease=Pituitary hormone deficiency; Pituitary hormone deficiency
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000008566.2; RCV000030379.1
|CLNDSDB=GeneReviews:MedGen:OMIM; MedGen
|CLNDSDBID=NBK1347:C0878683:262600; C1868294
|GENEINFO=PROP1:5626
|GENE_ID=5626
|GENE_NAME=PROP1
|CLNSRCID=601538.0002
}}{{PMID Auto
|PMID=106758
|Title=[Repeated intrauterine fetal death in a woman with genotype Rh-D-/-D-].
}}

{{PMID Auto
|PMID=9745452
|Title=The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiency.
}}

{{PMID Auto
|PMID=12414875
|Title=Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes.
}}

{{PMID Auto
|PMID=15519252
|Title=Pituitary hormone deficiencies due to transcription factor gene alterations.
}}

{{PMID Auto
|PMID=16984240
|Title=PROP1 gene analysis in Portuguese patients with combined pituitary hormone deficiency.
}}