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Variant (rsID / SNP)

rs140221307

IL17RA

rs140221307 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL17RA. Location: chromosome 22, position 17,586,757. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

IL17RAConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
22:17586757
Cytoband
22q11.1
HGVS
NM_014339.7(IL17RA):c.958T>C (p.Trp320Arg)
Allele change
Missense_W320R

Associated conditions / phenotypes

Familial Candidiasis, Recessive|Immunodeficiency 51

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.