rs1585717154
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
8
Location
71199380
Variant Type
SNP
Genes
LOC105375894
Phenotypes
ClinVar
Name
NM_000503.6(EYA1):c.1739T>G (p.Leu580Arg)
Allele
C
Clinical Significance
Likely pathogenic