Variants
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rs141996352

  • Benign

Your Genotype

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Description

Reference Allele

T


Alternative Allele

G

Chromosome

2


Location

219147735


Variant Type

SNP

Genes

ClinVar

Name

NM_024782.3(NHEJ1):c.451A>C (p.Arg151=)


Allele

G


Clinical Significance

Benign

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