rs769791060
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
10
Location
78021680
Variant Type
SNP
Genes
ClinVar
Name
NM_007055.4(POLR3A):c.1051C>T (p.Arg351Ter)
Allele
A
Clinical Significance
Pathogenic