rs794727814
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
13
Location
38784647
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.5858A>G (p.Asp1953Gly)
Allele
G
Clinical Significance
Uncertain significance