rs1229558573
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
11
Location
65554202
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001130144.3(LTBP3):c.510G>A (p.Pro170=)
Allele
T
Clinical Significance
Likely benign