rs754451669
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
8
Location
67746118
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_020361.5(CPA6):c.12C>T (p.Leu4=)
Allele
A
Clinical Significance
Likely benign