rs542074736
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
13
Location
38874595
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.8281+9C>T
Allele
T
Clinical Significance
Likely benign