Variants
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rs767385060

  • Uncertain significance

Your Genotype

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Description

Reference Allele

G


Alternative Allele

A

Chromosome

16


Location

2089836


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_001009944.3(PKD1):c.12803C>T (p.Pro4268Leu)


Allele

A


Clinical Significance

Uncertain significance

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