rs1557794917
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
1
Location
115732904
Variant Type
SNP
Genes
ClinVar
Name
NM_001232.4(CASQ2):c.603A>G (p.Lys201=)
Allele
C
Clinical Significance
Uncertain significance