rs777363402
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
1
Location
115727018
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001232.4(CASQ2):c.711G>A (p.Leu237=)
Allele
T
Clinical Significance
Likely benign