Variant (rsID / SNP)
rs3109650
rs3109650 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HACD2. Location: chromosome 3, position 123,298,615. The table records no clinical significance for this variant.
Reference-table entries
HACD2Not classified
- Variant type
- missense_variant&splice_region_variant
- Chromosome / position
- 3:123298615
- HGVS
- NM_001329783.2,c.275A>G,p.Asn92Ser
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.