rs768261470
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
1
Location
115725551
Variant Type
SNP
Genes
ClinVar
Name
NM_001232.4(CASQ2):c.740C>G (p.Pro247Arg)
Allele
C
Clinical Significance
Uncertain significance