rs1358873743
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
12
Location
32638702
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.2361T>G (p.Leu787=)
Allele
G
Clinical Significance
Likely benign