rs771823743
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
C
Chromosome
11
Location
65719787
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_032193.4(RNASEH2C):c.491A>T (p.Asp164Val)
Allele
A
Clinical Significance
Uncertain significance