rs771910342
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
12
Location
32625740
Variant Type
SNP
Genes
ClinVar
Name
NM_001370298.3(FGD4):c.2133A>G (p.Ala711=)
Allele
G
Clinical Significance
Likely benign