rs761798969
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
1
Location
115705207
Variant Type
SNP
Genes
ClinVar
Name
NM_001232.4(CASQ2):c.924G>A (p.Pro308=)
Allele
T
Clinical Significance
Uncertain significance