rs794727940
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
13
Location
38848468
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.6177A>G (p.Thr2059=)
Allele
G
Clinical Significance
Uncertain significance