rs137853318
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
X
Location
154367732
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001110556.2(FLNA):c.629G>T (p.Cys210Phe)
Allele
A
Clinical Significance
Pathogenic