rs150007765
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
T
Chromosome
13
Location
38864589
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.7966A>T (p.Ile2656Phe)
Allele
T
Clinical Significance
Likely benign