Variant (rsID / SNP)

rs587776682

rs587776682 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PROP1. Location: chromosome 5, position 177,421,325. Clinical significance in the table: Pathogenic.

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Reference-table entries

PROP1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Deletion
Chromosome / position: 5:177421325
Cytoband: 5q35.3
HGVS: NM_006261.5(PROP1):c.112_124del (p.Ser38fs)

Associated conditions / phenotypes

Pituitary hormone deficiency, combined, 2

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.