rs78599884
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
11
Location
65654381
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_021975.4(RELA):c.1653C>T (p.Ser551=)
Allele
A
Clinical Significance
Benign