rs890755853
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
10
Location
78021855
Variant Type
SNP
Genes
ClinVar
Name
NM_007055.4(POLR3A):c.1048+5G>T
Allele
A
Clinical Significance
Likely pathogenic