rs779675895
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
G
T
Chromosome
10
Location
78019173
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_007055.4(POLR3A):c.1278G>A (p.Thr426=)
Allele
T
Clinical Significance
Likely benign