rs267606816
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
X
Location
154367403
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001110556.2(FLNA):c.862G>A (p.Gly288Arg)
Allele
T
Clinical Significance
Pathogenic