Variants
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rs1057519204

  • Uncertain significance

Your Genotype

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Description

Reference Allele

G


Alternative Allele

C

Chromosome

22


Location

37973782


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_006941.4(SOX10):c.1114C>G (p.Gln372Glu)


Allele

C


Clinical Significance

Uncertain significance

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