Variant (rsID / SNP)

rs11200638

rs11200638 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HTRA1. Location: chromosome 10, position 124,220,544. Clinical significance in the table: risk factor.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

HTRA1Risk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 10:124220544
Cytoband: 10q26.13
HGVS: NM_002775.4(HTRA1):c.-625G>A

Associated conditions / phenotypes

Age related macular degeneration 7|Susceptibility to neovascular type of age-related macular degeneration

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.