rs1857352526
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
11
Location
65720355
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032193.4(RNASEH2C):c.235C>G (p.Leu79Val)
Allele
C
Clinical Significance
Uncertain significance