rs1341534652
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
12
Location
32625739
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.2132C>T (p.Ala711Val)
Allele
T
Clinical Significance
Uncertain significance