rs1589313663
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
10
Location
78009990
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_007055.4(POLR3A):c.1644T>C (p.Gly548=)
Allele
G
Clinical Significance
Likely benign