Variant (rsID / SNP)

rs226794

rs226794 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADAMTS5. Location: chromosome 21, position 28,302,355. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ADAMTS5Not classified

Variant type: missense_variant
Chromosome / position: 21:28302355
HGVS: NM_007038.5,c.2075T>C,p.Leu692Pro
Allele change: Missense_L692P

Associated conditions / phenotypes

Osteoarthritis|Ehlers-Danlos Syndrome|Back Pain

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.