Variant (rsID / SNP)
rs2229634
rs2229634 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ITPR3. Location: chromosome 6, position 33,638,180. The table records no clinical significance for this variant.
Reference-table entries
ITPR3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:33638180
- HGVS
- NM_002224.4,c.2268C>T,p.Gly756Gly
- Allele change
- Synonymous_G756G
Associated conditions / phenotypes
Graves' Disease|Autoimmune Disease|Kawasaki Disease|Vasculitis|Coronary Artery Aneurysm|Aneurysm|Squamous Cell Carcinoma|Cervical Squamous Cell Carcinoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.