Variant (rsID / SNP)

rs13184107

rs13184107 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL31RA. Location: chromosome 5, position 55,178,976. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

IL31RANot classified

Variant type: missense_variant
Chromosome / position: 5:55178976
HGVS: NM_139017.7,c.559G>A,p.Asp187Asn
Allele change: Missense_D187N

Associated conditions / phenotypes

Missense_D45N|Missense_D168N

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.