rs1589316371
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
10
Location
78017606
Variant Type
SNP
Genes
ClinVar
Name
NM_007055.4(POLR3A):c.1400C>T (p.Ser467Leu)
Allele
A
Clinical Significance
Uncertain significance