rs2553663
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
G
T
Chromosome
8
Location
67746398
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_020361.4(CPA6):c.-269G>A
Allele
T
Clinical Significance
Likely benign