rs781078327
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
11
Location
65553213
Variant Type
SNP
Genes
ClinVar
Name
NM_001130144.3(LTBP3):c.1014C>T (p.Gly338=)
Allele
A
Clinical Significance
Likely benign