rs1351119633
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
X
Location
154366193
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1260C>T (p.Ile420=)
Allele
A
Clinical Significance
Likely benign