rs782121971
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
X
Location
154366417
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1119C>G (p.Tyr373Ter)
Allele
C
Clinical Significance
Likely pathogenic