rs1590782835
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
11
Location
65552149
Variant Type
SNP
Genes
ClinVar
Name
NM_001130144.3(LTBP3):c.1354A>G (p.Lys452Glu)
Allele
C
Clinical Significance
Uncertain significance