Variants
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rs1332625359

  • Uncertain significance

Your Genotype

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Description

This variant was classified as: Uncertain significance. The following ACMG criteria were applied in classifying this variant: PM2,PP3.

Reference Allele

T


Alternative Allele

G

Chromosome

22


Location

37974178


Variant Type

SNP

Genes

ClinVar

Name

NM_006941.4(SOX10):c.718A>C (p.Thr240Pro)


Allele

G


Clinical Significance

Uncertain significance

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