rs112480709
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
8
Location
71197426
Variant Type
SNP
Genes
LOC105375894
ClinVar
Name
NM_000503.5(EYA1):c.*1914T>G
Allele
C
Clinical Significance
Likely benign