rs372865933
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
Chromosome
1
Location
115701395
Variant Type
SNP
Genes
ClinVar
Name
NM_001232.4(CASQ2):c.1046A>T (p.Asp349Val)
Allele
A
Clinical Significance
Uncertain significance