Variants
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rs1363663761

  • Likely benign

Your Genotype

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Description

Reference Allele

G


Alternative Allele

A

C

Chromosome

16


Location

2090479


Variant Type

SNP

Genes

ClinVar

Name

NM_001009944.3(PKD1):c.12250C>T (p.Pro4084Ser)


Allele

A


Clinical Significance

Likely benign

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