rs143082293
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
10
Location
78025065
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_007055.4(POLR3A):c.396C>T (p.Pro132=)
Allele
A
Clinical Significance
Likely benign