rs1554594182
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
8
Location
71211245
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_000503.6(EYA1):c.1609T>C (p.Cys537Arg)
Allele
G
Clinical Significance
Uncertain significance