Variants
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rs61737841

  • Benign

Your Genotype

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Description

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

ClinVar

Name

NM_001039141.3(TRIOBP):c.6899T>C (p.Val2300Ala)


Allele

C


Clinical Significance

Benign

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