rs759366601
- Uncertain significance
Your Genotype
Sign InDescription
This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Reference Allele
G
Alternative Allele
A
Chromosome
10
Location
78029422
Variant Type
SNP
Genes
ClinVar
Name
NM_007055.4(POLR3A):c.-15C>T
Allele
A
Clinical Significance
Uncertain significance