rs753988910
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
12
Location
32625063
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.2041G>A (p.Val681Ile)
Allele
A
Clinical Significance
Uncertain significance