rs1566169711
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
13
Location
38859591
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.7519+1G>A
Allele
A
Clinical Significance
Pathogenic
G
A
13
38859591
SNP
NM_207361.6(FREM2):c.7519+1G>A
A
Pathogenic