rs115054860
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
13
Location
38859430
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.7359G>A (p.Val2453=)
Allele
A
Clinical Significance
Benign