Variant (rsID / SNP)

rs11913443

rs11913443 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL17RA. Location: chromosome 22, position 17,594,977. Clinical significance in the table: Likely benign.

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Reference-table entries

IL17RALikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 22:17594977
Cytoband: 22q11.1
HGVS: NM_014339.7(IL17RA):c.*4267A>G
Allele change: Silent

Associated conditions / phenotypes

Familial Candidiasis, Recessive

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.