Variants
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rs1064797205

  • Likely pathogenic

Your Genotype

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Description

Reference Allele

C


Alternative Allele

G

T

Chromosome

16


Location

2089956


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_001009944.3(PKD1):c.12683G>C (p.Arg4228Pro)


Allele

G


Clinical Significance

Likely pathogenic

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