rs1857361152
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
11
Location
65720658
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032193.4(RNASEH2C):c.101G>A (p.Cys34Tyr)
Allele
T
Clinical Significance
Uncertain significance