rs267608670
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
10
Location
78007761
Variant Type
SNP
Genes
ClinVar
Name
NM_007055.4(POLR3A):c.2015G>A (p.Gly672Glu)
Allele
T
Clinical Significance
Pathogenic