rs115149211
- Benign/Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
13
Location
38880348
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.9071A>G (p.Asn3024Ser)
Allele
G
Clinical Significance
Benign/Likely benign