rs138139146
- Benign/Likely benign
Your Genotype
Sign InDescription
This variant is associated with the following publications: (PMID: 26969326, 28089734, 29197352)
Glu2246Lys in Exon 21 of TRIOBP: This variant is not expected to have clinical s ignificance because it has been identified in 0.5% (37/6742) of European America n chromosomes from a broad population by the NHLBI Exome Sequencing Project (htt p://evs.gs.washington.edu/EVS; dbSNP rs138139146).
Reference Allele
G
Alternative Allele
A
Chromosome
22
Location
37769262
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001039141.3(TRIOBP):c.6736G>A (p.Glu2246Lys)
Allele
A
Clinical Significance
Benign/Likely benign