Variants
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rs61737839

  • Benign

Your Genotype

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Description

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

ClinVar

Name

NM_001039141.3(TRIOBP):c.7032G>A (p.Glu2344=)


Allele

A


Clinical Significance

Benign

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