rs777365329
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
219157536
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024782.3(NHEJ1):c.326G>A (p.Arg109Gln)
Allele
T
Clinical Significance
Uncertain significance