rs34019581
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
10
Location
78009879
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_007055.4(POLR3A):c.1755G>A (p.Pro585=)
Allele
T
Clinical Significance
Likely benign