rs782684339
- Benign/Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
X
Location
154365246
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1581C>T (p.Arg527=)
Allele
A
Clinical Significance
Benign/Likely benign