rs375463904
- Likely benign
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
X
Location
154366077
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1376C>T (p.Thr459Met)
Allele
A
Clinical Significance
Likely benign
Name
NM_001110556.2(FLNA):c.1376C>A (p.Thr459Lys)
Allele
T
Clinical Significance
Uncertain significance