rs28935470
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
X
Location
154367505
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.760G>A (p.Glu254Lys)
Allele
T
Clinical Significance
Pathogenic
C
T
X
154367505
SNP
NM_001110556.2(FLNA):c.760G>A (p.Glu254Lys)
T
Pathogenic