rs1564623882
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
10
Location
78024970
Variant Type
SNP
Genes
ClinVar
Name
NM_007055.4(POLR3A):c.490+1G>A
Allele
T
Clinical Significance
Pathogenic
C
T
10
78024970
SNP
NM_007055.4(POLR3A):c.490+1G>A
T
Pathogenic