rs117063418
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
11
Location
65552969
Variant Type
SNP
Genes
ClinVar
Name
NM_001130144.3(LTBP3):c.1077C>T (p.Cys359=)
Allele
A
Clinical Significance
Benign
G
A
11
65552969
SNP
NM_001130144.3(LTBP3):c.1077C>T (p.Cys359=)
A
Benign