rs559353292
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
11
Location
65658806
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_021975.4(RELA):c.576C>T (p.Ala192=)
Allele
A
Clinical Significance
Likely benign