Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs5517

KLK1

rs5517 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KLK1. Location: chromosome 19, position 51,323,232. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

KLK1Not classified
Variant type
missense_variant
Chromosome / position
19:51323232
HGVS
NM_002257.4,c.556A>G,p.Lys186Glu
Allele change
Missense_K186E

Associated conditions / phenotypes

Hypertension, Essential|Colorectal Cancer|Adenoma

Public references

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