Variant (rsID / SNP)

rs3743781

rs3743781 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYLD. Location: chromosome 16, position 50,831,256. Clinical significance in the table: Benign.

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Reference-table entries

CYLDBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:50831256
Cytoband: 16q12.1
HGVS: NM_001378743.1(CYLD):c.*837A>G
Allele change: Silent

Associated conditions / phenotypes

Familial multiple trichoepitheliomata|Familial cylindromatosis|Brooke-Spiegler syndrome

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.