rs121434355
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
13
Location
38784709
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.5920G>A (p.Glu1974Lys)
Allele
A
Clinical Significance
Pathogenic