rs1060499603
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
8
Location
71211239
Variant Type
SNP
Genes
ClinVar
Name
NM_000503.6(EYA1):c.1615G>T (p.Glu539Ter)
Allele
A
Clinical Significance
Likely pathogenic