Variants
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rs749087938

  • Likely benign

Your Genotype

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Description

Reference Allele

C


Alternative Allele

A

G

Chromosome

16


Location

2090270


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_001009944.3(PKD1):c.12444+15G>C


Allele

G


Clinical Significance

Likely benign

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