Variants
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rs61729060

  • Benign

Your Genotype

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Description

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

ClinVar

Name

NM_001039141.3(TRIOBP):c.6806A>G (p.Asn2269Ser)


Allele

G


Clinical Significance

Benign

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