rs769960615
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
T
Chromosome
1
Location
115705198
Variant Type
SNP
Genes
ClinVar
Name
NM_001232.4(CASQ2):c.933T>A (p.Phe311Leu)
Allele
T
Clinical Significance
Uncertain significance