rs374741888
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
13
Location
38880276
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.9007-8C>T
Allele
T
Clinical Significance
Likely benign