rs372871850
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
11
Location
65662069
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_021975.4(RELA):c.54C>T (p.Gly18=)
Allele
A
Clinical Significance
Likely benign