Variants
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rs371118329

  • Likely benign

Your Genotype

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Description

Ser2264Ser in Exon 21 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 1/3292 African Amer ican chromosomes from a broad population by the NHLBI Exome Sequencing Project ( http://evs.gs.washington.edu/EVS).

Reference Allele

G


Alternative Allele

A

Chromosome

22


Location

37769318


Variant Type

SNP

Genes

ClinVar

Name

NM_001039141.3(TRIOBP):c.6792G>A (p.Ser2264=)


Allele

A


Clinical Significance

Likely benign

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