rs760696455
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
G
Chromosome
12
Location
32625052
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.2030T>G (p.Ile677Ser)
Allele
G
Clinical Significance
Uncertain significance