rs147067921
- Conflicting interpretations of pathogenicity
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
T
Chromosome
8
Location
67746069
Variant Type
SNP
Genes
ClinVar
Name
NM_020361.5(CPA6):c.61T>A (p.Phe21Ile)
Allele
T
Clinical Significance
Conflicting interpretations of pathogenicity