Variant (rsID / SNP)

rs6780995

rs6780995 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL17RD. Location: chromosome 3, position 57,138,419. The table records no clinical significance for this variant.

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Reference-table entries

IL17RDNot classified

Variant type: missense_variant
Chromosome / position: 3:57138419
HGVS: NM_017563.5,c.764C>T,p.Thr255Met
Allele change: Missense_T111M

Associated conditions / phenotypes

Malaria|Cytokine Deficiency

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.