Variants
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rs73415876

  • Pathogenic
  • Benign/Likely benign

Your Genotype

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Description

Reference Allele

G


Alternative Allele

A

C

T

Chromosome

22


Location

37983536


Variant Type

SNP

Genes

ClinVar

Name

NM_006941.4(SOX10):c.249C>G (p.Tyr83Ter)


Allele

C


Clinical Significance

Pathogenic

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