rs978710698
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
X
Location
154366648
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.988-9C>T
Allele
A
Clinical Significance
Likely benign
G
A
X
154366648
SNP
NM_001110556.2(FLNA):c.988-9C>T
A
Likely benign