Variants
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rs886038422

  • Likely benign

Your Genotype

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Description

Reference Allele

G


Alternative Allele

A

Chromosome

1


Location

115738264


Variant Type

SNP

Genes

ClinVar

Name

NM_001232.4(CASQ2):c.492C>T (p.Tyr164=)


Allele

A


Clinical Significance

Likely benign

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