Variant (rsID / SNP)

rs116225539

rs116225539 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PROP1. Location: chromosome 5, position 177,419,291. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PROP1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:177419291
Cytoband: 5q35.3
HGVS: NM_006261.5(PROP1):c.*419C>T
Allele change: Silent

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.