Variant (rsID / SNP)

rs2232228

rs2232228 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HAS3. Location: chromosome 16, position 69,143,577. Clinical significance in the table: drug_response.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

HAS3Drug response

Clinical significance (as recorded): drug_response
Variant type: synonymous_variant
Chromosome / position: 16:69143577
HGVS: NM_001199280.2,c.279A>G,p.Ala93Ala
Allele change: Synonymous_A93A

Associated conditions / phenotypes

Atrial Standstill 1

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.