rs782178449
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
X
Location
154366750
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.969G>A (p.Pro323=)
Allele
T
Clinical Significance
Benign
C
A
T
X
154366750
SNP
NM_001110556.2(FLNA):c.969G>A (p.Pro323=)
T
Benign