rs121909196
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
8
Location
71216733
Variant Type
SNP
Genes
ClinVar
Name
NM_000503.6(EYA1):c.1319G>A (p.Arg440Gln)
Allele
T
Clinical Significance
Pathogenic
C
T
8
71216733
SNP
NM_000503.6(EYA1):c.1319G>A (p.Arg440Gln)
T
Pathogenic