Variants
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rs1932482770

  • Likely pathogenic

Your Genotype

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Description

Reference Allele

T


Alternative Allele

C

Chromosome

22


Location

37983784


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_006941.4(SOX10):c.1A>G (p.Met1Val)


Allele

C


Clinical Significance

Likely pathogenic

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