rs1315056698
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
X
Location
154365453
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1463G>A (p.Arg488Gln)
Allele
T
Clinical Significance
Uncertain significance