Variant (rsID / SNP)

rs2289778

rs2289778 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KALRN. Location: chromosome 3, position 124,044,949. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

KALRNNot classified

Variant type: synonymous_variant
Chromosome / position: 3:124044949
HGVS: NM_001024660.5,c.1209C>T,p.Phe403Phe
Allele change: Synonymous_F403F

Associated conditions / phenotypes

Synonymous_F403F|Synonymous_F403F

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.