rs779006717
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
10
Location
78021621
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_007055.4(POLR3A):c.1110G>A (p.Ser370=)
Allele
T
Clinical Significance
Likely benign