rs796052116
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
11
Location
65554291
Variant Type
SNP
Genes
ClinVar
Name
NM_001130144.3(LTBP3):c.421C>T (p.Gln141Ter)
Allele
A
Clinical Significance
Pathogenic