Variants
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rs117661715

  • 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

C


Alternative Allele

A

G

T

Chromosome

19


Location

7631533


Variant Type

SNP

Genes

ClinVar

Name

NM_001171155.2(PET100):c.199C>T (p.Arg67Cys)


Allele

T


Clinical Significance

Benign

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