Variants
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rs1588054854

  • Uncertain significance

Your Genotype

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Description

Reference Allele

G


Alternative Allele

A

Chromosome

9


Location

110800959


Variant Type

SNP

Genes

ClinVar

Name

NM_005592.4(MUSK):c.2581G>A (p.Glu861Lys)


Allele

A


Clinical Significance

Uncertain significance

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