Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs4253325

KLKB1

rs4253325 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KLKB1. Location: chromosome 4, position 187,178,473. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

KLKB1Not classified
Variant type
missense_variant
Chromosome / position
4:187178473
HGVS
NM_000892.5,c.1679G>A,p.Arg560Gln
Allele change
Missense_R560Q

Associated conditions / phenotypes

Hypertension, Essential

Public references

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