rs757866333
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
11
Location
65720050
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_032193.4(RNASEH2C):c.463G>A (p.Ala155Thr)
Allele
T
Clinical Significance
Uncertain significance