rs1472614573
- Pathogenic
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
10
Location
78009953
Variant Type
SNP
Genes
ClinVar
Name
NM_007055.4(POLR3A):c.1681C>T (p.Arg561Ter)
Allele
A
Clinical Significance
Pathogenic
Name
NM_007055.4(POLR3A):c.1681C>G (p.Arg561Gly)
Allele
C
Clinical Significance
Likely pathogenic