rs886044820
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
X
Location
154367674
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001110556.2(FLNA):c.687G>T (p.Met229Ile)
Allele
A
Clinical Significance
Uncertain significance