rs1647217312
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
C
Chromosome
1
Location
115717841
Variant Type
SNP
Genes
ClinVar
Name
NM_001232.4(CASQ2):c.837A>T (p.Pro279=)
Allele
A
Clinical Significance
Uncertain significance
Name
NM_001232.4(CASQ2):c.837A>G (p.Pro279=)
Allele
C
Clinical Significance
Uncertain significance