rs782539251
- Conflicting interpretations of pathogenicity
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
X
Location
154365429
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1487G>A (p.Arg496Gln)
Allele
T
Clinical Significance
Conflicting interpretations of pathogenicity