rs138538977
- Benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
10
Location
78010538
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_007055.4(POLR3A):c.1575T>G (p.Thr525=)
Allele
C
Clinical Significance
Benign