rs782067087
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
X
Location
154365218
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1609G>A (p.Val537Met)
Allele
T
Clinical Significance
Uncertain significance
Name
NM_001110556.2(FLNA):c.1609G>C (p.Val537Leu)
Allele
G
Clinical Significance
Uncertain significance