Variants
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rs2091436717

  • Uncertain significance

Your Genotype

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Description

PM2, PP3, PP4

Reference Allele

A


Alternative Allele

C

Chromosome

16


Location

2090343


Variant Type

SNP

Genes

ClinVar

Name

NM_001009944.3(PKD1):c.12386T>G (p.Met4129Arg)


Allele

C


Clinical Significance

Uncertain significance

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