rs1404084092
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
12
Location
32607996
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.1444A>G (p.Met482Val)
Allele
G
Clinical Significance
Uncertain significance