rs1280215477
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
G
Chromosome
1
Location
115738215
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001232.4(CASQ2):c.532+9T>G
Allele
C
Clinical Significance
Likely benign