Variants
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rs4134809

  • Benign

Your Genotype

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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

G


Alternative Allele

A

C

T

Chromosome

19


Location

7629507


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_020196.3(XAB2):c.21C>T (p.Leu7=)


Allele

A


Clinical Significance

Benign

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