rs267608678
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
10
Location
78025043
Variant Type
SNP
Genes
ClinVar
Name
NM_007055.4(POLR3A):c.418C>T (p.Arg140Ter)
Allele
A
Clinical Significance
Pathogenic
G
A
10
78025043
SNP
NM_007055.4(POLR3A):c.418C>T (p.Arg140Ter)
A
Pathogenic