Variant (rsID / SNP)
rs17167553
rs17167553 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRGUK. Location: chromosome 7, position 133,848,257. The table records no clinical significance for this variant.
Reference-table entries
LRGUKNot classified
- Variant type
- missense_variant
- Chromosome / position
- 7:133848257
- HGVS
- NM_001365700.3,c.904G>T,p.Asp302Tyr
- Allele change
- Missense_D302Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.