rs371909600
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
X
Location
154364882
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1767C>T (p.Gly589=)
Allele
A
Clinical Significance
Benign
G
A
X
154364882
SNP
NM_001110556.2(FLNA):c.1767C>T (p.Gly589=)
A
Benign