rs1592515601
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
Chromosome
12
Location
32640411
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.2590C>G (p.Leu864Val)
Allele
G
Clinical Significance
Uncertain significance