rs200008207
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
8
Location
71215634
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_000503.6(EYA1):c.1455A>C (p.Ala485=)
Allele
G
Clinical Significance
Likely benign