rs371600068
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
X
Location
154366817
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.902G>T (p.Arg301Leu)
Allele
A
Clinical Significance
Uncertain significance