rs199523517
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
10
Location
78009918
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_007055.4(POLR3A):c.1716G>T (p.Leu572=)
Allele
A
Clinical Significance
Likely benign