rs1338845809
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
T
Chromosome
13
Location
38783152
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.5724A>G (p.Gly1908=)
Allele
G
Clinical Significance
Likely benign