Variants
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rs61729063

  • Benign

Your Genotype

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Description

His2191Tyr in Exon 19 of TRIOBP: This variant is not expected to have clinical s ignificance because it has been identified in 1.7% (57/3300) of African American chromosomes from a broad population by the NHLBI Exome Sequencing Project (http ://evs.gs.washington.edu/EVS; dbSNP rs61729063).

Reference Allele

C


Alternative Allele

T

Chromosome

22


Location

37768172


Variant Type

SNP

Genes

ClinVar

Name

NM_001039141.3(TRIOBP):c.6571C>T (p.His2191Tyr)


Allele

T


Clinical Significance

Benign

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