rs786205177
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
X
Location
154365487
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1430-1G>T
Allele
A
Clinical Significance
Pathogenic
C
A
X
154365487
SNP
NM_001110556.2(FLNA):c.1430-1G>T
A
Pathogenic