rs782592312
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
G
Chromosome
X
Location
154366786
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.933T>G (p.Ala311=)
Allele
C
Clinical Significance
Likely benign