rs118204451
- Conflicting interpretations of pathogenicity
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
2
Location
219158194
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024782.3(NHEJ1):c.169C>G (p.Arg57Gly)
Allele
C
Clinical Significance
Conflicting interpretations of pathogenicity