rs114688149
- Conflicting interpretations of pathogenicity
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
13
Location
38880390
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.9113T>C (p.Val3038Ala)
Allele
C
Clinical Significance
Conflicting interpretations of pathogenicity