rs28935169
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
Chromosome
X
Location
154371001
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.245A>T (p.Glu82Val)
Allele
A
Clinical Significance
Pathogenic
T
A
X
154371001
SNP
NM_001110556.2(FLNA):c.245A>T (p.Glu82Val)
A
Pathogenic