Variants
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rs1932460904

  • Pathogenic

Your Genotype

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Description

Reference Allele

C


Alternative Allele

T

Chromosome

22


Location

37983356


Variant Type

SNP

Genes

ClinVar

Name

NM_006941.4(SOX10):c.428+1G>A


Allele

T


Clinical Significance

Pathogenic

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