rs1563630587
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
T
Chromosome
8
Location
71215501
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_000503.6(EYA1):c.1483T>A (p.Cys495Ser)
Allele
T
Clinical Significance
Likely pathogenic