rs28403592
- Conflicting interpretations of pathogenicity
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
11
Location
65553238
Variant Type
SNP
Genes
ClinVar
Name
NM_001130144.3(LTBP3):c.989C>T (p.Pro330Leu)
Allele
A
Clinical Significance
Conflicting interpretations of pathogenicity