Variants
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rs1373797370

  • Likely pathogenic

Your Genotype

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Description

Reference Allele

C


Alternative Allele

G

T

Chromosome

22


Location

37978112


Variant Type

SNP

Genes

ClinVar

Name

NM_006941.4(SOX10):c.452G>C (p.Arg151Pro)


Allele

G


Clinical Significance

Likely pathogenic

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