rs2067757148
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
X
Location
154366098
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001110556.2(FLNA):c.1355G>A (p.Gly452Asp)
Allele
T
Clinical Significance
Uncertain significance