rs1654321088
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
1
Location
115705194
Variant Type
SNP
Genes
ClinVar
Name
NM_001232.4(CASQ2):c.937C>G (p.Leu313Val)
Allele
C
Clinical Significance
Uncertain significance