rs1590792358
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
11
Location
65557921
Variant Type
SNP
Genes
ClinVar
Name
NM_001130144.3(LTBP3):c.39T>G (p.Pro13=)
Allele
C
Clinical Significance
Likely benign