Variants
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rs118204451

  • Conflicting interpretations of pathogenicity

Your Genotype

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Description

Reference Allele

G


Alternative Allele

A

C

Chromosome

2


Location

219158194


Variant Type

SNP

Genes

ClinVar

Name

NM_024782.3(NHEJ1):c.169C>G (p.Arg57Gly)


Allele

C


Clinical Significance

Conflicting interpretations of pathogenicity

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