rs142681516
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
2
Location
3558210
Variant Type
SNP
Genes
LOC100506054
Phenotypes
ClinVar
Name
NM_002936.6(RNASEH1):c.51C>T (p.Pro17=)
Allele
A
Clinical Significance
Likely benign