rs1585810834
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
8
Location
71215479
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_000503.6(EYA1):c.1505C>G (p.Thr502Ser)
Allele
C
Clinical Significance
Likely benign