rs533939591
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
12
Location
32602280
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.1367G>A (p.Arg456His)
Allele
A
Clinical Significance
Uncertain significance