rs756137476
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
G
Chromosome
11
Location
65552891
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001130144.3(LTBP3):c.1155T>C (p.His385=)
Allele
G
Clinical Significance
Likely benign