Variants
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rs772619751

  • Uncertain significance

Your Genotype

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Description

Reference Allele

T


Alternative Allele

C

G

Chromosome

1


Location

115701291


Variant Type

SNP

Genes

ClinVar

Name

NM_001232.4(CASQ2):c.1150A>G (p.Asn384Asp)


Allele

C


Clinical Significance

Uncertain significance

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