rs863223346
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
13
Location
38876091
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.8351G>A (p.Arg2784Lys)
Allele
A
Clinical Significance
Likely pathogenic