Variant (rsID / SNP)

rs767671406

rs767671406 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FLCN. Location: chromosome 17, position 17,119,820. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FLCNConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: Microsatellite
Chromosome / position: 17:17119820
Cytoband: 17p11.2
HGVS: NM_144997.7(FLCN):c.1177-5_1177-3del

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Multiple fibrofolliculomas

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.