rs61737839
- Benign
Your Genotype
Sign InDescription
Glu2344Glu in Exon 23 of TRIOBP: This variant is not expected to have clinical s ignificance because it does not alter an amino acid residue, is not located with in the splice consensus sequence, and has been identified in 1.8% (67/3684) of A frican American chromosomes from a broad population by the NHLBI Exome Sequencin g Project (http://evs.gs.washington.edu/EVS; dbSNP rs61737839).
Reference Allele
G
Alternative Allele
A
T
Chromosome
22
Location
37772696
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001039141.3(TRIOBP):c.7032G>A (p.Glu2344=)
Allele
A
Clinical Significance
Benign