Variant (rsID / SNP)

rs147873628

rs147873628 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL17F. Location: chromosome 6, position 52,101,830. Clinical significance in the table: Uncertain significance.

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Reference-table entries

IL17FUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 6:52101830
Cytoband: 6p12.2
HGVS: NM_052872.4(IL17F):c.391C>T (p.Arg131Trp)
Allele change: Missense_R131W

Associated conditions / phenotypes

Candidiasis, familial, 6

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.