rs121909201
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
8
Location
71215470
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_000503.6(EYA1):c.1514T>G (p.Leu505Arg)
Allele
C
Clinical Significance
Pathogenic