rs1589319208
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
10
Location
78024553
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_007055.4(POLR3A):c.641C>T (p.Ala214Val)
Allele
A
Clinical Significance
Uncertain significance