rs61737841
- Benign
Your Genotype
Sign InDescription
Val2300Ala in Exon 22 of TRIOBP: This variant is not expected to have clinical s ignificance because it has been identified in 1.8% (60/3292) of African American chromosomes from a broad population by the NHLBI Exome Sequencing Project (http ://evs.gs.washington.edu/EVS; dbSNP rs61737841).
Reference Allele
T
Alternative Allele
C
Chromosome
22
Location
37771699
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001039141.3(TRIOBP):c.6899T>C (p.Val2300Ala)
Allele
C
Clinical Significance
Benign