Variants
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rs980952719

  • Likely benign

Your Genotype

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Description

Reference Allele

G


Alternative Allele

C

Chromosome

9


Location

110785519


Variant Type

SNP

Genes

ClinVar

Name

NM_005592.4(MUSK):c.1587-8G>C


Allele

C


Clinical Significance

Likely benign

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