rs776008006
- Benign/Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
Chromosome
1
Location
115738342
Variant Type
SNP
Genes
ClinVar
Name
NM_001232.4(CASQ2):c.421-7A>T
Allele
A
Clinical Significance
Benign/Likely benign