rs779295406
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
11
Location
65720285
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032193.4(RNASEH2C):c.305C>T (p.Ser102Phe)
Allele
A
Clinical Significance
Uncertain significance