rs1555216969
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
T
Chromosome
12
Location
32608061
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.1509G>T (p.Leu503Phe)
Allele
T
Clinical Significance
Uncertain significance