Variants
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rs34689457

  • Benign

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Description

This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.

Reference Allele

C


Alternative Allele

A

T

Chromosome

2


Location

219158323


Variant Type

SNP

Genes

ClinVar

Name

NM_024782.3(NHEJ1):c.40G>A (p.Ala14Thr)


Allele

T


Clinical Significance

Benign

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