Variants
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rs1555939415

  • Likely pathogenic
  • Likely pathogenic

Your Genotype

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Description

Reference Allele

T


Alternative Allele

C

G

Chromosome

22


Location

37983382


Variant Type

SNP

Genes

ClinVar

Name

NM_006941.4(SOX10):c.403A>C (p.Ser135Arg)


Allele

G


Clinical Significance

Likely pathogenic

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