rs1563630117
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
8
Location
71215386
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_000503.6(EYA1):c.1597+1G>A
Allele
T
Clinical Significance
Pathogenic
C
T
8
71215386
SNP
NM_000503.6(EYA1):c.1597+1G>A
T
Pathogenic