rs773830258
- Uncertain significance
Your Genotype
Sign InDescription
This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Reference Allele
G
Alternative Allele
C
Chromosome
11
Location
65720703
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032193.4(RNASEH2C):c.56C>G (p.Ala19Gly)
Allele
C
Clinical Significance
Uncertain significance