rs144892779
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
10
Location
78019224
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_007055.4(POLR3A):c.1227A>G (p.Gln409=)
Allele
C
Clinical Significance
Benign