Variant (rsID / SNP)
rs2229515
rs2229515 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TJP1. Location: chromosome 15, position 30,018,627. The table records no clinical significance for this variant.
Reference-table entries
TJP1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 15:30018627
- HGVS
- NM_001301025.3,c.2647A>G,p.Ile883Val
- Allele change
- Missense_I790V
Associated conditions / phenotypes
Missense_I883V|Missense_I790V|Missense_I790V|Missense_I794V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.