Variant (rsID / SNP)

rs115419420

rs115419420 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL17RC. Location: chromosome 3, position 9,970,121. Clinical significance in the table: Benign.

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Reference-table entries

IL17RCBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:9970121
Cytoband: 3p25.3
HGVS: NM_153460.4(IL17RC):c.1010C>T (p.Pro337Leu)
Allele change: Missense_P337L

Associated conditions / phenotypes

Candidiasis, familial, 9

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.