rs184864998
- 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
Lines of evidence used in support of classification: General population or subpopulation frequency is too high to be a pathogenic mutation based on disease/syndrome prevalence and penetrance
Reference Allele
T
Alternative Allele
C
Chromosome
X
Location
154366837
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.882A>G (p.Thr294=)
Allele
C
Clinical Significance
Benign