rs373878188
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
13
Location
38850123
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.6465T>C (p.Asp2155=)
Allele
C
Clinical Significance
Likely benign