rs1592515619
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
Chromosome
12
Location
32640412
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.2591T>A (p.Leu864Gln)
Allele
A
Clinical Significance
Uncertain significance