rs1172505050
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
X
Location
154367439
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.826C>T (p.Arg276Trp)
Allele
A
Clinical Significance
Uncertain significance