rs764981765
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
11
Location
65552397
Variant Type
SNP
Genes
ClinVar
Name
NM_001130144.3(LTBP3):c.1196C>T (p.Pro399Leu)
Allele
A
Clinical Significance
Uncertain significance