rs121909197
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
8
Location
71211215
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_000503.6(EYA1):c.1639A>G (p.Arg547Gly)
Allele
C
Clinical Significance
Pathogenic