rs771013055
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
11
Location
65719800
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_032193.4(RNASEH2C):c.478C>T (p.Gln160Ter)
Allele
A
Clinical Significance
Likely pathogenic