rs782114616
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
X
Location
154364825
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1824G>A (p.Thr608=)
Allele
T
Clinical Significance
Benign
C
A
T
X
154364825
SNP
NM_001110556.2(FLNA):c.1824G>A (p.Thr608=)
T
Benign