rs138360068
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
T
Chromosome
8
Location
67746111
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_020361.5(CPA6):c.19C>T (p.Arg7Cys)
Allele
A
Clinical Significance
Uncertain significance