rs886044791
- Conflicting interpretations of pathogenicity
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
X
Location
154366429
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1107C>T (p.Pro369=)
Allele
A
Clinical Significance
Conflicting interpretations of pathogenicity