rs142377910
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
12
Location
32640452
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.2631A>G (p.Thr877=)
Allele
G
Clinical Significance
Likely benign