rs745468085
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
13
Location
38877191
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.8619G>A (p.Leu2873=)
Allele
A
Clinical Significance
Likely benign