Variants
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rs1057522682

  • Likely 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

C

Chromosome

19


Location

7629815


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_001171155.2(PET100):c.-19G>C


Allele

C


Clinical Significance

Likely benign

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