Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs2297322

SLC15A1

rs2297322 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC15A1. Location: chromosome 13, position 99,376,181. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

SLC15A1Not classified
Variant type
missense_variant
Chromosome / position
13:99376181
HGVS
NM_005073.4,c.350G>A,p.Ser117Asn
Allele change
Missense_S117N

Associated conditions / phenotypes

Ileitis|Allergic Disease|Inflammatory Bowel Disease|Proteasome-Associated Autoinflammatory Syndrome 1|Gastritis

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.