Variant (rsID / SNP)

rs878855218

rs878855218 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FLCN. Location: chromosome 17, position 17,124,943. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

FLCNLikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 17:17124943
Cytoband: 17p11.2
HGVS: NM_144997.7(FLCN):c.780-1G>C
Allele change: Silent

Associated conditions / phenotypes

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.