rs141834289
- Benign/Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
13
Location
38872858
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.8100T>G (p.Leu2700=)
Allele
G
Clinical Significance
Benign/Likely benign