rs747321858
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
10
Location
78022235
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_007055.4(POLR3A):c.795C>T (p.Ser265=)
Allele
A
Clinical Significance
Likely benign