rs781889196
- Benign/Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
X
Location
154366761
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.958G>A (p.Val320Met)
Allele
T
Clinical Significance
Benign/Likely benign