rs145657148
- Conflicting interpretations of pathogenicity
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
13
Location
38880286
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.9009C>T (p.Val3003=)
Allele
T
Clinical Significance
Conflicting interpretations of pathogenicity