rs368732492
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
13
Location
38874511
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.8206G>A (p.Gly2736Ser)
Allele
A
Clinical Significance
Uncertain significance