rs371092631
- Benign/Likely benign
Your Genotype
Sign InDescription
General population or subpopulation frequency is too high to be a pathogenic mutation based on disease/syndrome prevalence and penetrance
Reference Allele
G
Alternative Allele
A
Chromosome
X
Location
154367533
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.732C>T (p.Pro244=)
Allele
A
Clinical Significance
Benign/Likely benign