Variants
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rs200313246

  • Uncertain significance

Your Genotype

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Description

In silico analysis, which includes protein predictors and evolutionary conservation, supports a deleterious effect

This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

Reference Allele

A


Alternative Allele

T

Chromosome

22


Location

37769084


Variant Type

SNP

Genes

ClinVar

Name

NM_001039141.3(TRIOBP):c.6632A>T (p.Gln2211Leu)


Allele

T


Clinical Significance

Uncertain significance

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