Variant (rsID / SNP)

rs199932303

rs199932303 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL36RN. Location: chromosome 2, position 113,820,090. Clinical significance in the table: Uncertain significance.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

IL36RNUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 2:113820090
Cytoband: 2q14.1
HGVS: NM_012275.3(IL36RN):c.304C>T (p.Arg102Trp)
Allele change: Missense_R102W

Associated conditions / phenotypes

Generalized pustular psoriasis

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.