rs2067762985
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
X
Location
154366561
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1065+1G>T
Allele
A
Clinical Significance
Likely pathogenic