rs1808471410
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
8
Location
71211258
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_000503.6(EYA1):c.1598-2A>G
Allele
C
Clinical Significance
Pathogenic
T
C
8
71211258
SNP
NM_000503.6(EYA1):c.1598-2A>G
C
Pathogenic