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Mutation:
FREM2 A199S
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
FRASER SYNDROME 2
Minor Allele Frequency: (ESP6500)
[0.0847]
Minor Allele Frequency: (1000 Genomes)
[0.139776]
External references
dbSNP:
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