Variants
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rs767794127

  • Uncertain significance

Your Genotype

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Description

Reference Allele

C


Alternative Allele

G

T

Chromosome

1


Location

930203


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_001385641.1(SAMD11):c.658C>T (p.Arg220Trp)


Allele

T


Clinical Significance

Uncertain significance

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