rs368320173
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
8
Location
71211204
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_000503.6(EYA1):c.1650G>A (p.Val550=)
Allele
T
Clinical Significance
Likely benign