rs141996352
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
2
Location
219147735
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024782.3(NHEJ1):c.451A>C (p.Arg151=)
Allele
G
Clinical Significance
Benign
T
G
2
219147735
SNP
NM_024782.3(NHEJ1):c.451A>C (p.Arg151=)
G
Benign