rs1557178932
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
C
Chromosome
X
Location
154365214
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1613A>G (p.Tyr538Cys)
Allele
C
Clinical Significance
Uncertain significance