rs763729954
- Uncertain significance
Your Genotype
Sign InDescription
RELA NM_021975.3 exon 10 p.Arg336Arg (c.1008C>T):This variant has not been reported in the literature and is not present in large control databases. Evolutionary conservation and computational predictive tools for this variant are limited or unavailable. Of note, this variant is a silent variant and does not change the amino acid, reducing the probability that this variant is disease causing. In summary, data on this variant is insufficient for disease classification. Therefore, the clinical significance of this variant is uncertain.
Reference Allele
G
Alternative Allele
A
T
Chromosome
11
Location
65655713
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_021975.4(RELA):c.1008C>T (p.Arg336=)
Allele
A
Clinical Significance
Uncertain significance