Variants
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rs1601879005

  • Likely benign

Your Genotype

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Description

Reference Allele

G


Alternative Allele

C

Chromosome

22


Location

37973867


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_006941.4(SOX10):c.1029C>G (p.Pro343=)


Allele

C


Clinical Significance

Likely benign

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