rs770571012
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
1
Location
115738333
Variant Type
SNP
Genes
ClinVar
Name
NM_001232.4(CASQ2):c.423A>G (p.Leu141=)
Allele
C
Clinical Significance
Likely benign