rs2067771137
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
X
Location
154367484
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.781C>G (p.Leu261Val)
Allele
C
Clinical Significance
Uncertain significance