Variant (rsID / SNP)
rs2293948
rs2293948 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TBC1D25. The table records no clinical significance for this variant.
Reference-table entries
TBC1D25Not classified
- Variant type
- missense_variant
- HGVS
- NM_001348262.2,c.878A>G,p.Asn293Ser
- Allele change
- Missense_N293S
Associated conditions / phenotypes
Silent|Missense_N219S|Missense_N219S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.