rs1363246020
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
11
Location
65654507
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_021975.4(RELA):c.1527G>A (p.Arg509=)
Allele
T
Clinical Significance
Likely benign