rs201590889
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
11
Location
65553761
Variant Type
SNP
Genes
ClinVar
Name
NM_001130144.3(LTBP3):c.804C>T (p.Pro268=)
Allele
A
Clinical Significance
Benign
G
A
C
11
65553761
SNP
NM_001130144.3(LTBP3):c.804C>T (p.Pro268=)
A
Benign