rs1020313300
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
13
Location
38784599
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.5810C>T (p.Ser1937Phe)
Allele
T
Clinical Significance
Uncertain significance