rs928398769
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
12
Location
32608006
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.1454C>A (p.Pro485His)
Allele
A
Clinical Significance
Uncertain significance