rs755558916
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
1
Location
115732926
Variant Type
SNP
Genes
ClinVar
Name
NM_001232.4(CASQ2):c.581A>C (p.Lys194Thr)
Allele
G
Clinical Significance
Uncertain significance