rs754901033
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
8
Location
71215461
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_000503.6(EYA1):c.1523C>T (p.Ala508Val)
Allele
A
Clinical Significance
Uncertain significance