rs1437502609
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
13
Location
38850198
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.6540C>T (p.Arg2180=)
Allele
T
Clinical Significance
Likely benign