rs772062656
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
11
Location
65552153
Variant Type
SNP
Genes
ClinVar
Name
NM_001130144.3(LTBP3):c.1350G>A (p.Ala450=)
Allele
T
Clinical Significance
Likely benign