Variants
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rs1641746770

  • Uncertain significance

Your Genotype

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Description

Reference Allele

C


Alternative Allele

T

Chromosome

1


Location

941236


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_001385641.1(SAMD11):c.1288C>T (p.Arg430Cys)


Allele

T


Clinical Significance

Uncertain significance

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