rs61759893
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
11
Location
65658293
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_021975.4(RELA):c.871G>A (p.Asp291Asn)
Allele
T
Clinical Significance
Benign
C
T
11
65658293
SNP
NM_021975.4(RELA):c.871G>A (p.Asp291Asn)
T
Benign