Variants
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rs756330364

  • Uncertain significance

Your Genotype

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Description

Reference Allele

G


Alternative Allele

A

C

Chromosome

22


Location

37769175


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_001039141.3(TRIOBP):c.6723G>C (p.Leu2241=)


Allele

C


Clinical Significance

Uncertain significance

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