rs16935547
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
10
Location
78025023
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_007055.4(POLR3A):c.438C>T (p.Ile146=)
Allele
A
Clinical Significance
Benign
G
A
10
78025023
SNP
NM_007055.4(POLR3A):c.438C>T (p.Ile146=)
A
Benign