rs2067774568
- Likely pathogenic
Your Genotype
Sign InDescription
This variant was classified as: Likely pathogenic. This variant was detected in hemizygous state.
Reference Allele
C
Alternative Allele
G
Chromosome
X
Location
154367837
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001110556.2(FLNA):c.622+5G>C
Allele
G
Clinical Significance
Likely pathogenic