rs1648031031
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
1
Location
115738224
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001232.4(CASQ2):c.532T>C (p.Tyr178His)
Allele
G
Clinical Significance
Uncertain significance