rs1593459578
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
13
Location
38877128
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.8556A>G (p.Pro2852=)
Allele
G
Clinical Significance
Likely benign