rs1603362942
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
X
Location
154366649
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.988-10C>T
Allele
A
Clinical Significance
Likely benign
G
A
X
154366649
SNP
NM_001110556.2(FLNA):c.988-10C>T
A
Likely benign