Variants
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rs770571012

  • Likely benign

Your Genotype

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Description

Reference Allele

T


Alternative Allele

C

Chromosome

1


Location

115738333


Variant Type

SNP

Genes

ClinVar

Name

NM_001232.4(CASQ2):c.423A>G (p.Leu141=)


Allele

C


Clinical Significance

Likely benign

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