rs200792226
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
11
Location
65720392
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032193.4(RNASEH2C):c.198C>T (p.Arg66=)
Allele
A
Clinical Significance
Benign