rs1857359953
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
11
Location
65720617
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032193.4(RNASEH2C):c.142T>C (p.Phe48Leu)
Allele
G
Clinical Significance
Uncertain significance