rs546487084
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
10
Location
78026183
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_007055.4(POLR3A):c.91C>T (p.Gln31Ter)
Allele
A
Clinical Significance
Pathogenic