Variant (rsID / SNP)
rs2074505
rs2074505 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GNL1. Location: chromosome 6, position 30,521,137. The table records no clinical significance for this variant.
Reference-table entries
GNL1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:30521137
- HGVS
- NM_005275.5,c.798C>T,p.Asp266Asp
- Allele change
- Synonymous_D266D
Associated conditions / phenotypes
Graves' Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.