rs754879716
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
1
Location
115738282
Variant Type
SNP
Genes
ClinVar
Name
NM_001232.4(CASQ2):c.474C>T (p.Phe158=)
Allele
A
Clinical Significance
Likely benign