rs768328161
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
13
Location
38878941
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.8970T>C (p.Ser2990=)
Allele
C
Clinical Significance
Likely benign