Variants
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rs63749871

  • Conflicting interpretations of pathogenicity
  • Pathogenic

Your Genotype

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Description

Reference Allele

T


Alternative Allele

C

G

Chromosome

12


Location

32602217


Variant Type

SNP

Genes

ClinVar

Name

NM_001370298.3(FGD4):c.1304T>C (p.Met435Thr)


Allele

C


Clinical Significance

Conflicting interpretations of pathogenicity

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