rs374178459
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
13
Location
38848563
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.6272C>T (p.Ala2091Val)
Allele
T
Clinical Significance
Uncertain significance