rs768786804
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
12
Location
32638745
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.2404G>A (p.Val802Met)
Allele
A
Clinical Significance
Uncertain significance