Variant (rsID / SNP)
rs61984162
rs61984162 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGHA2. Location: chromosome 14, position 106,054,456. The table records no clinical significance for this variant.
Reference-table entries
IGHA2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 14:106054456
- HGVS
- unassigned_transcript_2421,c.276T>C,p.Ile92Ile
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.