rs750159744
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
1
Location
115744858
Variant Type
SNP
Genes
ClinVar
Name
NM_001232.4(CASQ2):c.289A>G (p.Lys97Glu)
Allele
C
Clinical Significance
Uncertain significance