Variants
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rs1569169289

  • Pathogenic

Your Genotype

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Description

Reference Allele

G


Alternative Allele

A

T

Chromosome

22


Location

37978077


Variant Type

SNP

Genes

ClinVar

Name

NM_006941.4(SOX10):c.487C>T (p.Gln163Ter)


Allele

A


Clinical Significance

Pathogenic

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