Variants
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rs74315515

  • Pathogenic
  • Pathogenic/Likely pathogenic

Your Genotype

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Description

Reference Allele

C


Alternative Allele

G

T

Chromosome

22


Location

37983381


Variant Type

SNP

Genes

ClinVar

Name

NM_006941.4(SOX10):c.404G>C (p.Ser135Thr)


Allele

G


Clinical Significance

Pathogenic

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