Variant (rsID / SNP)

rs3803761

rs3803761 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FLCN. Location: chromosome 17, position 17,116,412. Clinical significance in the table: Benign.

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Reference-table entries

FLCNBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:17116412
Cytoband: 17p11.2
HGVS: NM_144997.7(FLCN):c.*557T>C
Allele change: Silent

Associated conditions / phenotypes

Multiple fibrofolliculomas|Familial spontaneous pneumothorax

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.