Variants
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rs397515457

  • Pathogenic

Your Genotype

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Description

Reference Allele

A


Alternative Allele

C

Chromosome

22


Location

37983783


Variant Type

SNP

Genes

ClinVar

Name

NM_006941.4(SOX10):c.2T>G (p.Met1Arg)


Allele

C


Clinical Significance

Pathogenic

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