Variants
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rs138515231

  • Benign

Your Genotype

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Description

Reference Allele

T


Alternative Allele

C

Chromosome

2


Location

219158327


Variant Type

SNP

Genes

ClinVar

Name

NM_024782.3(NHEJ1):c.36A>G (p.Pro12=)


Allele

C


Clinical Significance

Benign

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