Variants
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rs754976866

  • Uncertain significance

Your Genotype

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Description

Reference Allele

C


Alternative Allele

T

Chromosome

9


Location

110800717


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_005592.4(MUSK):c.2339C>T (p.Thr780Ile)


Allele

T


Clinical Significance

Uncertain significance

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