rs1360400826
- Uncertain significance
Your Genotype
Sign InDescription
This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Reference Allele
A
Alternative Allele
G
Chromosome
X
Location
154366104
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001110556.2(FLNA):c.1349T>C (p.Met450Thr)
Allele
G
Clinical Significance
Uncertain significance