rs61729060
- Benign
Your Genotype
Sign InDescription
Asn2269Ser in Exon 21 of TRIOBP: This variant is not expected to have clinical s ignificance because it has been identified in 1.6% (54/3292) of African American chromosomes from a broad population by the NHLBI Exome Sequencing Project (http ://evs.gs.washington.edu/EVS; dbSNP rs61729060).
Reference Allele
A
Alternative Allele
G
Chromosome
22
Location
37769332
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001039141.3(TRIOBP):c.6806A>G (p.Asn2269Ser)
Allele
G
Clinical Significance
Benign