rs767978562
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
13
Location
38851093
Variant Type
SNP
Genes
ClinVar
Name
NM_207361.6(FREM2):c.6727C>T (p.Arg2243Ter)
Allele
T
Clinical Significance
Pathogenic