Variants
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rs1601886662

  • Likely pathogenic

Your Genotype

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Description

Reference Allele

A


Alternative Allele

G

Chromosome

22


Location

37983355


Variant Type

SNP

Genes

ClinVar

Name

NM_006941.4(SOX10):c.428+2T>C


Allele

G


Clinical Significance

Likely pathogenic

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