rs782475689
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
T
Chromosome
X
Location
154366783
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.936C>A (p.Gly312=)
Allele
T
Clinical Significance
Likely benign