rs138515231
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
2
Location
219158327
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024782.3(NHEJ1):c.36A>G (p.Pro12=)
Allele
C
Clinical Significance
Benign
T
C
2
219158327
SNP
NM_024782.3(NHEJ1):c.36A>G (p.Pro12=)
C
Benign