Variant (rsID / SNP)
rs2291258
rs2291258 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GOLGA3. Location: chromosome 12, position 133,378,440. The table records no clinical significance for this variant.
Reference-table entries
GOLGA3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 12:133378440
- HGVS
- NM_001389683.1,c.1713G>A,p.Leu571Leu
- Allele change
- Synonymous_L571L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.