rs775405769
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
G
Chromosome
10
Location
78024588
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_007055.4(POLR3A):c.606A>G (p.Glu202=)
Allele
C
Clinical Significance
Likely benign