rs1566175991
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
13
Location
38877184
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.8612T>C (p.Leu2871Pro)
Allele
C
Clinical Significance
Uncertain significance