rs1326268854
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
11
Location
65658790
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_021975.4(RELA):c.592C>T (p.Arg198Ter)
Allele
A
Clinical Significance
Likely pathogenic