Variants
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rs1447190013

  • Likely benign

Your Genotype

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Description

Reference Allele

A


Alternative Allele

G

Chromosome

9


Location

110800889


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_005592.4(MUSK):c.2511A>G (p.Leu837=)


Allele

G


Clinical Significance

Likely benign

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