rs2082190695
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
12
Location
32602303
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.1390G>A (p.Val464Ile)
Allele
A
Clinical Significance
Uncertain significance