rs201941540
- Benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
11
Location
65552909
Variant Type
SNP
Genes
ClinVar
Name
NM_001130144.3(LTBP3):c.1137T>C (p.Cys379=)
Allele
G
Clinical Significance
Benign
A
G
11
65552909
SNP
NM_001130144.3(LTBP3):c.1137T>C (p.Cys379=)
G
Benign