rs765610331
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
G
Chromosome
10
Location
78004892
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_007055.4(POLR3A):c.2075-4A>C
Allele
G
Clinical Significance
Likely benign