rs782226711
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
X
Location
154366015
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1429+9G>A
Allele
T
Clinical Significance
Likely benign
C
T
X
154366015
SNP
NM_001110556.2(FLNA):c.1429+9G>A
T
Likely benign