rs72939112
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
11
Location
65552241
Variant Type
SNP
Genes
ClinVar
Name
NM_001130144.3(LTBP3):c.1345+7C>T
Allele
A
Clinical Significance
Likely benign
G
A
T
11
65552241
SNP
NM_001130144.3(LTBP3):c.1345+7C>T
A
Likely benign