Variant (rsID / SNP)

rs16910526

rs16910526 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLEC7A. Location: chromosome 12, position 10,271,087. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CLEC7ABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:10271087
Cytoband: 12p13.2
HGVS: NM_197947.3(CLEC7A):c.714T>G (p.Tyr238Ter)
Allele change: Silent

Associated conditions / phenotypes

Familial chronic mucocutaneous candidiasis|Aspergillosis, susceptibility to

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.