rs772757667
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
11
Location
65720343
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032193.4(RNASEH2C):c.247G>A (p.Val83Met)
Allele
T
Clinical Significance
Uncertain significance