rs121909200
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
8
Location
71215630
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_000503.6(EYA1):c.1459T>C (p.Ser487Pro)
Allele
G
Clinical Significance
Pathogenic