rs372782469
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
13
Location
38784793
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.6004C>T (p.Pro2002Ser)
Allele
T
Clinical Significance
Uncertain significance