rs145461540
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
13
Location
38880287
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.9010G>A (p.Ala3004Thr)
Allele
A
Clinical Significance
Likely benign