Variants
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rs193214210

  • Benign

Your Genotype

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Description

Reference Allele

A


Alternative Allele

G

Chromosome

9


Location

110800910


Variant Type

SNP

Genes

ClinVar

Name

NM_005592.4(MUSK):c.2532A>G (p.Ala844=)


Allele

G


Clinical Significance

Benign

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