rs118203973
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
T
Chromosome
12
Location
32625774
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.2167G>T (p.Gly723Ter)
Allele
T
Clinical Significance
Pathogenic