rs1249067213
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
2
Location
219157511
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024782.3(NHEJ1):c.351C>G (p.Phe117Leu)
Allele
C
Clinical Significance
Uncertain significance