rs142684479
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
2
Location
219158191
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024782.3(NHEJ1):c.172G>T (p.Ala58Ser)
Allele
A
Clinical Significance
Uncertain significance