Variant (rsID / SNP)
rs56166910
rs56166910 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HAS1. Location: chromosome 19, position 52,223,180. The table records no clinical significance for this variant.
Reference-table entries
HAS1Not classified
- Variant type
- intron_variant
- Chromosome / position
- 19:52223180
- HGVS
- NM_001523.4,c.10-29T>C
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.