rs370490152
- Likely pathogenic
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
X
Location
154366582
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1045G>T (p.Glu349Ter)
Allele
A
Clinical Significance
Likely pathogenic
Name
NM_001110556.2(FLNA):c.1045G>A (p.Glu349Lys)
Allele
T
Clinical Significance
Likely benign