rs1385540267
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
13
Location
38861427
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.7520-4C>A
Allele
A
Clinical Significance
Likely benign