rs1847614190
- Uncertain significance
Your Genotype
Sign InDescription
This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Reference Allele
A
Alternative Allele
T
Chromosome
10
Location
78024617
Variant Type
SNP
Genes
ClinVar
Name
NM_007055.4(POLR3A):c.577T>A (p.Phe193Ile)
Allele
T
Clinical Significance
Uncertain significance