rs368041880
- Benign/Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
X
Location
154364818
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1828+3A>G
Allele
C
Clinical Significance
Benign/Likely benign