rs375013523
- Benign/Likely benign
Your Genotype
Sign InDescription
Leu2247Leu in Exon 21 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 0.6% (19/3346) of A frican American chromosomes from a broad population by the NHLBI Exome Sequencin g Project (http://evs.gs.washington.edu/EVS).
Reference Allele
G
Alternative Allele
A
Chromosome
22
Location
37769267
Variant Type
SNP
Genes
ClinVar
Name
NM_001039141.3(TRIOBP):c.6741G>A (p.Leu2247=)
Allele
A
Clinical Significance
Benign/Likely benign