Variants
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rs1555938395

  • Pathogenic/Likely pathogenic

Your Genotype

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Description

Reference Allele

G


Alternative Allele

A

Chromosome

22


Location

37978041


Variant Type

SNP

Genes

ClinVar

Name

NM_006941.4(SOX10):c.523C>T (p.Pro175Ser)


Allele

A


Clinical Significance

Pathogenic/Likely pathogenic

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