Variants
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rs727503531

  • Likely benign

Your Genotype

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Description

*2+10G>A in intron 23 of TRIOBP: This variant is not expected to have clinical s ignificance because it is not located within the splice consensus sequence and i s not predicted to impact splicing.

Reference Allele

G


Alternative Allele

A

Chromosome

22


Location

37772774


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_001039141.3(TRIOBP):c.*2+10G>A


Allele

A


Clinical Significance

Likely benign

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