rs782670288
- Conflicting interpretations of pathogenicity
Your Genotype
Sign InDescription
This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Reference Allele
C
Alternative Allele
T
Chromosome
X
Location
154367745
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.623-7G>A
Allele
T
Clinical Significance
Conflicting interpretations of pathogenicity