rs754600353
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
T
Chromosome
12
Location
32608087
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.1535A>T (p.Asp512Val)
Allele
T
Clinical Significance
Uncertain significance