rs1557798151
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
1
Location
115740766
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001232.4(CASQ2):c.382G>A (p.Glu128Lys)
Allele
T
Clinical Significance
Uncertain significance