rs757027564
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
G
Chromosome
10
Location
78025609
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_007055.4(POLR3A):c.318+13G>C
Allele
G
Clinical Significance
Uncertain significance