rs1557180178
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
X
Location
154370908
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.338T>C (p.Phe113Ser)
Allele
G
Clinical Significance
Uncertain significance