rs782155641
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
X
Location
154364900
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1749C>T (p.Gly583=)
Allele
A
Clinical Significance
Benign
G
A
X
154364900
SNP
NM_001110556.2(FLNA):c.1749C>T (p.Gly583=)
A
Benign