rs141899032
- Uncertain significance
Your Genotype
Sign InDescription
This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Reference Allele
C
Alternative Allele
A
T
Chromosome
10
Location
78021884
Variant Type
SNP
Genes
ClinVar
Name
NM_007055.4(POLR3A):c.1024G>T (p.Val342Phe)
Allele
A
Clinical Significance
Uncertain significance