rs138226409
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
11
Location
65659769
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_021975.4(RELA):c.456C>T (p.Tyr152=)
Allele
A
Clinical Significance
Benign
G
A
11
65659769
SNP
NM_021975.4(RELA):c.456C>T (p.Tyr152=)
A
Benign