rs202221935
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
11
Location
65552992
Variant Type
SNP
Genes
ClinVar
Name
NM_001130144.3(LTBP3):c.1064-10C>T
Allele
A
Clinical Significance
Benign
G
A
11
65552992
SNP
NM_001130144.3(LTBP3):c.1064-10C>T
A
Benign