rs1857351791
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
11
Location
65720329
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032193.4(RNASEH2C):c.261A>C (p.Glu87Asp)
Allele
G
Clinical Significance
Uncertain significance