{{Rsnum
|rsid=7445271
|Gene=PROP1
|Chromosome=5
|position=177995875
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.001377
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{Venter SNP
|rsid=7445271
|allele=C
|frequency=
|uid=1103654304212
|type=homozygous_SNP
|hugo=PROP1
|ensembl gene=ENSG00000175325
|ensembl transcript=ENST00000308304
|sift=TOLERATED
|disease=Defects in PROP1 are a cause of combined pituitary hormone deficiency (CPHD) (MIM:601538, 262600). It is characterized by impaired production of growth hormone (GH) and one or more of the other five anterior pituitary hormones.
}}

{{GET Evidence
|gene=PROP1
|aa_change=Asn20Ser
|aa_change_short=N20S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7445271
|overall_frequency_n=10752
|overall_frequency_d=10756
|overall_frequency=0.999628
|n_genomes=47
|n_genomes_annotated=0
|n_haplomes=94
|n_articles=1
|n_articles_annotated=1
|qualityscore_in_silico=4
|qualitycomment_in_silico=Y
|gene_in_genetests=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=0
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}