Variants
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rs606231342

  • Likely pathogenic

Your Genotype

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Description

Regulation of SOX10 expression

Reference Allele

G


Alternative Allele

A

Chromosome

22


Location

38016208


Variant Type

SNP

Genes

ClinVar

Name

NM_001301130.2(POLR2F):c.453-24860G>A


Allele

A


Clinical Significance

Likely pathogenic

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