Variant (rsID / SNP)
rs3827440
rs3827440 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPR174. The table records no clinical significance for this variant.
Reference-table entries
GPR174Not classified
- Variant type
- missense_variant
- HGVS
- NM_032553.3,c.484T>C,p.Ser162Pro
- Allele change
- Missense_S162P
Associated conditions / phenotypes
Graves' Disease|Hypothyroidism|Thyroid Gland Disease|Autoimmune Disease|Hyperthyroidism|Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.